16990674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445768-G-A

16990674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445768-G-T

16990700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445794-G-A

16990700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445794-G-C

16990700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445794-G-T

16990743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445812-G-A

16990743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445812-G-C

16990743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445812-G-T

http://identifiers.org/hco/12/GRCh38#16990771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445840-C-A

16990771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445840-C-G

16990771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445840-C-T

http://identifiers.org/hco/12/GRCh38#16990777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445846-A-C

16990777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445846-A-G

16990778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445847-A-G

16990780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445849-A-G

16990780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445849-A-T

http://identifiers.org/hco/12/GRCh38#16990787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445856-C-A

16990787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445856-C-G

16990787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445856-C-T

16990795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445864-T-A

16990822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445891-G-A

16990822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445891-G-C

16990822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445891-G-T

16990837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445906-T-C

http://identifiers.org/hco/12/GRCh38#16990839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445908-C-A

16990839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445908-C-G

16990839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445908-C-T

16990841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445910-T-C

16990849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445918-G-A

16990849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445918-G-T

16990852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445921-T-A

16990862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445931-G-A

16990862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445931-G-T

16990869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445938-A-G

http://identifiers.org/hco/12/GRCh38#16990874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445943-C-A

16990874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445943-C-T

http://identifiers.org/hco/12/GRCh38#16990885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445954-C-A

16990887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445956-T-C

16990891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445960-T-C

http://identifiers.org/hco/12/GRCh38#16990898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445967-C-A

16990898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445967-C-G

16990898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445967-C-T

16990909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445978-T-G

16990921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445990-G-A

16990921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445990-G-C

http://identifiers.org/hco/12/GRCh38#16990927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445996-C-A

16990927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40445996-C-T

16990933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446002-T-A

16990934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446003-A-G

http://identifiers.org/hco/12/GRCh38#16990945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446014-C-A

16990945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446014-C-T

http://identifiers.org/hco/12/GRCh38#16990953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446022-A-C

http://identifiers.org/hco/12/GRCh38#16990954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446023-C-A

16990954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446023-C-T

16990958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446027-G-C

16990958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446027-G-T

http://identifiers.org/hco/12/GRCh38#16990963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446032-C-A

16990963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446032-C-T

16990964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446033-A-G

16990964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446033-A-T

http://identifiers.org/hco/12/GRCh38#16990966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446035-C-A

16990974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446043-T-C

16990984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446053-G-A

16990984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446053-G-T

16990990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446059-T-C

http://identifiers.org/hco/12/GRCh38#16990991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446060-C-A

16990991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446060-C-T

http://identifiers.org/hco/12/GRCh38#16990992-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446061-A-C

16990992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446061-A-G

16990992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446061-A-T

16990994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446063-G-A

16990994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446063-G-T

http://identifiers.org/hco/12/GRCh38#16991008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446077-C-A

16991011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446080-G-A

16991011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446080-G-T

16991015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446084-G-A

16991015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446084-G-T

16991033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446102-G-T

16991039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446108-G-A

16991053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446122-C-T

16991059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446128-T-A

16991060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446129-G-A

16991060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446129-G-T

16991061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446130-G-T

16991070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446139-A-G

16991071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446140-T-A

16991071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446140-T-G

16991072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446141-G-A

16991072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446141-G-C

16991072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446141-G-T

16991096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446165-C-T

16991107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446176-A-G

16991107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446176-A-T

16991143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446212-T-A

16991143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446212-T-C

http://identifiers.org/hco/12/GRCh38#16991152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446221-C-A

16991152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446221-C-G

http://identifiers.org/hco/12/GRCh38#16991158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446227-C-A

16991158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446227-C-T

16991170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446239-T-A

16991170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446239-T-C

16991171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446240-G-A

16991171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446240-G-T

http://identifiers.org/hco/12/GRCh38#16991179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446248-C-A

16991179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446248-C-T

16991180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446249-G-A

16991180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446249-G-T

16991224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446293-T-C

16991246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446315-A-T

16991282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446351-A-G

http://identifiers.org/hco/12/GRCh38#16991290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446359-C-A

16991290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446359-C-T

16991293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446362-G-A

16991293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446362-G-T

16991305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446374-G-T

16991315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446384-G-A

16991315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446384-G-T

16991323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446392-T-A

16991326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446395-G-C

16991326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446395-G-T

16991334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446403-A-G

http://identifiers.org/hco/12/GRCh38#16991338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446407-C-A

16991338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446407-C-T

http://identifiers.org/hco/12/GRCh38#16991344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446413-A-C

16991344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446413-A-T

http://identifiers.org/hco/12/GRCh38#16991349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446418-C-A

16991349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446418-C-T

http://identifiers.org/hco/12/GRCh38#16991351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446420-C-A

16991351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446420-C-G

16991351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446420-C-T

16991353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446422-G-A

16991353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446422-G-T

16991355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446424-T-C

16991362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446431-T-C

http://identifiers.org/hco/12/GRCh38#16991363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446432-C-A

16991363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446432-C-G

http://identifiers.org/hco/12/GRCh38#16991368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446437-C-A

16991368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446437-C-T

16991369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446438-T-C

16991369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446438-T-G

http://identifiers.org/hco/12/GRCh38#16991375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446444-C-A

16991375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446444-C-T

16991377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446446-A-G

http://identifiers.org/hco/12/GRCh38#16991387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446456-C-A

16991387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446456-C-G

16991387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446456-C-T

http://identifiers.org/hco/12/GRCh38#16991390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446459-C-A

16991390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446459-C-T

16991424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446493-A-G

16991424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446493-A-T

http://identifiers.org/hco/12/GRCh38#16991465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446533-C-A

16991465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446533-C-T

16991478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446546-G-A

16991478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446546-G-C

16991478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446546-G-T

16991489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446557-A-G

http://identifiers.org/hco/12/GRCh38#16991490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446558-C-A

http://identifiers.org/hco/12/GRCh38#16991509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446587-C-A

16991542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446620-A-G

16991559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446637-G-A

16991559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446637-G-T

16991561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446639-G-T

http://identifiers.org/hco/12/GRCh38#16991607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446685-C-A

16991607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446685-C-T

16991608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446686-T-C

16991612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446690-A-G

16991625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446703-A-T

16991653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446731-C-T

http://identifiers.org/hco/12/GRCh38#16991728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446806-C-A

16991728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446806-C-G

16991728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446806-C-T

16991746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446824-T-C

16991758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446836-T-C

16991796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446874-T-A

16991796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446874-T-C

16991811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446889-G-A

16991811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446889-G-C

16991811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446889-G-T

16991855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446934-G-A

16991855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446934-G-T

16991858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446937-G-A

16991858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446937-G-C

16991858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446937-G-T

16991866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446945-T-A

16991866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446945-T-C

16991870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446949-A-G

16991870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446949-A-T

16991875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446954-T-A

16991875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446954-T-C

16991889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446968-T-A

16991889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446968-T-C

16991889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446968-T-G

16991892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446971-G-A

16991892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446971-G-T

16991899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446978-G-A

16991899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446978-G-T

http://identifiers.org/hco/12/GRCh38#16991908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446987-A-C

16991909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446988-G-T

http://identifiers.org/hco/12/GRCh38#16991919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446998-C-A

16991919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446998-C-T

16991920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40446999-T-C

http://identifiers.org/hco/12/GRCh38#16991921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447000-C-A

16991921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447000-C-G

16991921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447000-C-T

16991923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447002-G-A

16991923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447002-G-C

16991923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447002-G-T

http://identifiers.org/hco/12/GRCh38#16991929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447008-C-A

16991929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447008-C-T

16991940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447019-G-T

16991944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447023-T-C

16991950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447029-A-G

http://identifiers.org/hco/12/GRCh38#16991951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447030-C-A

16991951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447030-C-G

16991953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447032-G-A

16991953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447032-G-T

16991954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447033-A-G

http://identifiers.org/hco/12/GRCh38#16991955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447034-C-A

16991955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447034-C-G

16991955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447034-C-T

http://identifiers.org/hco/12/GRCh38#16991962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447041-C-A

16991976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447055-A-T

16991980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447059-A-G

16991980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447059-A-T

16991993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447072-G-A

16991993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447072-G-T

16991996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447075-G-A

16991996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447075-G-T

16992006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447085-G-A

16992006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447085-G-T

http://identifiers.org/hco/12/GRCh38#16992015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447094-C-A

16992015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447094-C-G

16992015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447094-C-T

16992017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447096-A-G

16992017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447096-A-T

http://identifiers.org/hco/12/GRCh38#16992018-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447097-A-C

16992018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447097-A-G

16992055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447135-T-C

16992076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37889
most severe consequence: non coding transcript exon variant
orthologous variants: 40447156-G-T