58295221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non coding transcript exon variant
orthologous variants: 96303132-G-C

58295221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non coding transcript exon variant
orthologous variants: 96303132-G-T

http://identifiers.org/hco/16/GRCh38#58295228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96303139-C-A

58295228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non coding transcript exon variant
orthologous variants: 96303139-C-T

58295233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non coding transcript exon variant
orthologous variants: 96303144-G-T

http://identifiers.org/hco/16/GRCh38#58295249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96303158-C-A

58295249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non coding transcript exon variant
orthologous variants: 96303158-C-T

58295270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non coding transcript exon variant
orthologous variants: 96303178-A-G

58295270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non coding transcript exon variant
orthologous variants: 96303178-A-T

58295414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non coding transcript exon variant
orthologous variants: 96303261-T-G

http://identifiers.org/hco/16/GRCh38#58295484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96303320-C-A

58295494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non coding transcript exon variant
orthologous variants: 96303329-A-G

58295495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non coding transcript exon variant
orthologous variants: 96303330-G-A

http://identifiers.org/hco/16/GRCh38#58295609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96303435-C-A

58295609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96303435-C-G

58295642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96303466-G-A

58295642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96303466-G-T

58317750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96316718-G-T

http://identifiers.org/hco/16/GRCh38#58317766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96316733-C-A

58317784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96316757-C-T

58317792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96316765-G-A

http://identifiers.org/hco/16/GRCh38#58318350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#96317504-C-A

58318350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96317504-C-T

58318487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96317641-A-G

http://identifiers.org/hco/16/GRCh38#58319335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96317733-C-A

58319360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96317759-G-A

58319398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96317799-C-T

58319541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96317968-G-A

58319581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96318006-C-T

58324107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96319955-T-A

http://identifiers.org/hco/16/GRCh38#58324111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96319959-A-C

58324117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96319965-G-C

58324158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96320006-G-A

58324158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96320006-G-T

58324170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96320018-G-A

58324170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96320018-G-T

58324186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96320034-G-C

58324198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96320046-G-A

http://identifiers.org/hco/16/GRCh38#58324222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96320081-A-C

58324222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96320081-A-G

58324222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96320081-A-T

58324609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96320531-C-T

58324866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96321104-C-T

58325029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96321431-G-A

58325029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96321431-G-C

58325134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96321536-A-G

58325657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96322714-C-T

58325695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96322755-G-A

58325724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96322788-T-C

58325852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96322936-C-T

58325986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96323059-A-T

58326276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96323906-G-A

58326278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96323908-T-C

58326286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96323918-C-T

58330716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96326212-G-A

58330727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96326223-C-T

http://identifiers.org/hco/16/GRCh38#58330745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96326254-A-C

58330807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96326312-A-G

58331002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96326464-T-A

58331026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96326487-G-A

58331092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96326528-C-T

58336815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96326685-C-T

58337185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96327034-T-G

58337250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96327108-A-T

http://identifiers.org/hco/16/GRCh38#58337330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96327178-C-A

http://identifiers.org/hco/16/GRCh38#58337806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96327305-C-A

58337806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96327305-C-G

58339586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96327826-G-T

58339619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96327859-C-T

58339662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96327899-C-T

58339759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96327957-C-T

58339778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96327974-G-A

58339800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96327993-C-T

58345821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96333393-G-A

58347111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96334086-G-T

58347230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96334201-G-A

58347234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96334205-G-A

58347500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96334661-T-A

58348344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96335053-G-A

58348797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96336249-T-G

58348840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96336290-T-C

58348889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96336336-G-A

58348889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96336336-G-C

58348930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96336381-A-T

58348957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96336408-T-C

58348982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96336432-G-A

58349476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96336919-T-G

58349658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96337077-T-G

58349751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96337178-G-T

58349800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96337208-C-T

http://identifiers.org/hco/16/GRCh38#58350006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96337404-C-A

58351427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96337519-A-G

58351428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96337520-T-C

58351537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96337616-A-G

58351552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96337633-G-A

58351562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96337643-G-A

58351574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96337654-T-G

58351720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96337801-C-T

58351841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96337936-G-A

58352096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96338648-G-A

58352140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96338697-C-T

58352185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96338752-A-G

http://identifiers.org/hco/16/GRCh38#58352355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96338897-A-C

http://identifiers.org/hco/16/GRCh38#58352383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96338909-A-C

58352401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96338926-C-T

58366042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96342806-G-T

58366087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96342856-C-T

http://identifiers.org/hco/16/GRCh38#58366131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96342898-A-C

58366165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96342933-G-A

58366383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96343138-G-A

http://identifiers.org/hco/16/GRCh38#58366389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#96343144-C-A

58366389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96343144-C-T

58366468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96343227-C-T

58366472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96343231-A-G

58366531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96343292-A-G

58366569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96343329-G-A

http://identifiers.org/hco/16/GRCh38#58366695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96343439-A-C

http://identifiers.org/hco/16/GRCh38#58368040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96344857-C-A

58368040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96344857-C-T

http://identifiers.org/hco/16/GRCh38#58368041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96344858-C-A

58368041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96344858-C-T

http://identifiers.org/hco/16/GRCh38#58368056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96344874-C-A

58368056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96344874-C-T

58368081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96344899-G-A

58368112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96344934-T-C

58368186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96345006-A-G

http://identifiers.org/hco/16/GRCh38#58368252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96345057-C-A

58368252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96345057-C-T

58368268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96345073-G-C

58368268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96345073-G-T

58368276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 96345081-C-T

58368309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96345124-A-G

58368314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96345129-T-C

http://identifiers.org/hco/16/GRCh38#58368371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96345187-C-A

58368405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96345251-G-T

http://identifiers.org/hco/16/GRCh38#58368573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96345676-C-A

58368573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96345676-C-T

58368628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96345735-C-T

58368916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96346133-A-G

58368961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96346182-G-A

58368968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96346189-G-A

58369252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96346575-A-G

58369780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96346785-A-G

58369780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96346785-A-T

58370043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96347024-A-T

58370116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96347343-G-C

58370139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96347367-T-C

58370140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96347368-A-G

58370230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96347470-G-A

58370377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96347605-G-A

58370557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96347740-T-C

http://identifiers.org/hco/16/GRCh38#58370710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96347938-A-C

58370754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96348049-G-A

58370949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96348282-T-G

58371018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96348340-T-A

http://identifiers.org/hco/16/GRCh38#58371226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96348501-C-A

58381331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96352972-C-T

58381578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96353372-C-T

58381648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96353443-T-A

58385804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96354034-G-A

58385804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96354034-G-T

http://identifiers.org/hco/16/GRCh38#58385836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96354064-C-A

http://identifiers.org/hco/16/GRCh38#58387255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96354337-C-A

58387396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96354466-A-G

58387448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96354515-C-G

58387467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96354541-C-T

58387615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96354651-C-T

58387644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96354680-T-A

58387644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96354680-T-C

58389665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96356956-G-C

58390283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96357710-C-T

58390310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96357736-C-T

58391620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96359348-G-T

58391999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96359696-T-A

58392036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96359732-T-C

http://identifiers.org/hco/16/GRCh38#58392105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96359798-C-A

58392105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96359798-C-G

http://identifiers.org/hco/16/GRCh38#58392165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96359851-C-A

58392283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 96359962-G-T

http://identifiers.org/hco/16/GRCh38#58392292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#96359971-C-A

58392292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 96359971-C-T

http://identifiers.org/hco/16/GRCh38#58392339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#96360014-C-A

58392339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 96360014-C-T

http://identifiers.org/hco/16/GRCh38#58392348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#96360023-C-A

58392348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 96360023-C-T

http://identifiers.org/hco/16/GRCh38#58392351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#96360026-C-A

58392351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 96360026-C-G

http://identifiers.org/hco/16/GRCh38#58392415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#96360092-C-A

58392415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 96360092-C-T

58392423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 96360100-G-A

58392423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 96360100-G-T

58392495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 96360168-G-C

58392495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 96360168-G-T

58392538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96360194-A-G

58392538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96360194-A-T

58392643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96360267-G-A

http://identifiers.org/hco/16/GRCh38#58392793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#96360417-C-A

58392793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96360417-C-G

58392793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 96360417-C-T

58392809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96360423-C-G

58392809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96360423-C-T

http://identifiers.org/hco/16/GRCh38#58392836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96360459-C-A

58392836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96360459-C-G

58392836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96360459-C-T

58392866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96360499-G-A

58392960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 96360589-C-G

58392961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96360590-G-C

58393444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96361044-A-G

58393499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 96361100-C-T

58402268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron variant
orthologous variants: 96362546-G-A

http://identifiers.org/hco/16/GRCh38#58402329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96362598-A-C

http://identifiers.org/hco/16/GRCh38#58402388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96362650-A-C

58402477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron variant
orthologous variants: 96362737-G-T

58402838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron variant
orthologous variants: 96363281-G-C

58402838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron variant
orthologous variants: 96363281-G-T

58402883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron variant
orthologous variants: 96363307-G-T

58402894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron variant
orthologous variants: 96363318-T-C

http://identifiers.org/hco/16/GRCh38#58402931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96363355-C-A

58402931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron variant
orthologous variants: 96363355-C-G

58402931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron variant
orthologous variants: 96363355-C-T

58403298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96364638-C-G

58403298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96364638-C-T

58403389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96364718-A-G

58403389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96364718-A-T

http://identifiers.org/hco/16/GRCh38#58403581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96366862-C-A

58403581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96366862-C-T

58403607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96366884-G-A

58403607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96366884-G-T

58403842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96367002-T-C

http://identifiers.org/hco/16/GRCh38#58403853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96367013-C-A

58403853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96367013-C-T

http://identifiers.org/hco/16/GRCh38#58403854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96367014-C-A

58403857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96367021-C-G

58403879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96367043-T-C

58403879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96367043-T-G

58404467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96369709-A-G

http://identifiers.org/hco/16/GRCh38#58404474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96369715-C-A

58404474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96369715-C-G

58404474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 96369715-C-T

58404494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 96369730-C-G

58404494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 96369730-C-T

http://identifiers.org/hco/16/GRCh38#58404611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96369847-C-A

58404611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 96369847-C-T

58404717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 96369953-T-C

58404739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96369971-G-T

http://identifiers.org/hco/16/GRCh38#58404744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96369976-C-A

58404744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96369976-C-G

58404744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96369976-C-T

58404776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370003-G-C

58404804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370030-G-A

58404866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370088-G-A

58404866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370088-G-C

58404881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370104-G-A

http://identifiers.org/hco/16/GRCh38#58404902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96370125-C-A

58404935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370157-T-C

58404937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370159-A-G

58404976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370196-A-G

http://identifiers.org/hco/16/GRCh38#58405011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96370231-C-A

58405011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370231-C-T

58405017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370237-T-C

http://identifiers.org/hco/16/GRCh38#58405081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96370276-A-C

58405081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370276-A-T

58405119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370301-T-C

58405121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370303-G-A

58405121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370303-G-T

58405173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370356-T-C

http://identifiers.org/hco/16/GRCh38#58405228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96370386-C-A

58405268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370426-A-T

http://identifiers.org/hco/16/GRCh38#58405392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#96370538-C-A

58405424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370561-G-T

58405455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370590-C-T

58405472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96370606-A-G

58405646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96371314-C-G

58405692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96371360-G-T

58405824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96371501-G-A

58405824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96371501-G-T

58405931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25851
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 96371590-G-A