16824817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: 13281366-T-A

16824817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: 13281366-T-C

16824817-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: 13281366-T-G

16824830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: 13281379-T-C

16824830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: 13281379-T-G

16824879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: 13281427-T-A

http://identifiers.org/hco/10/GRCh38#16824886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13281434-C-A

16824886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: 13281434-C-T

http://identifiers.org/hco/10/GRCh38#16824925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13281472-C-A

16824928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: 13281480-G-T

16824930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: 13281482-G-A

16824930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: 13281482-G-T

http://identifiers.org/hco/10/GRCh38#16824945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13281496-A-C

16824945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: 13281496-A-G

16824961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: 13281513-G-A

16824961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: 13281513-G-C

16824961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3 prime UTR variant
orthologous variants: 13281513-G-T

16825010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13281574-G-A

16825194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13281756-G-T

16827335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13282703-T-A

http://identifiers.org/hco/10/GRCh38#16828754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13283103-A-C

16828795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13283160-T-G

16828884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13283252-C-G

16828980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13283348-G-A

16828985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13283353-T-C

16828985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13283353-T-G

16830504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13284376-G-A

16831129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13284757-A-G

16831129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13284757-A-T

16831256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13284891-G-A

16831388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13285023-T-A

16831388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13285023-T-C

16831391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13285026-T-C

16831391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13285026-T-G

16831468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13285121-A-G

16831471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13285124-T-A

16831471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13285124-T-C

16831669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13285374-C-T

16831700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13285404-G-C

http://identifiers.org/hco/10/GRCh38#16831712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13285416-C-A

16831860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13285543-G-A

16832143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13285654-C-T

http://identifiers.org/hco/10/GRCh38#16832410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13285825-C-A

16832523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13285918-A-T

16832574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13285999-T-C

16832623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13286047-G-A

16832636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13286060-A-G

16832770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13286161-G-C

16832793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13286183-C-T

16832819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13286207-C-G

http://identifiers.org/hco/10/GRCh38#16832850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13286237-C-A

16832850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13286237-C-T

http://identifiers.org/hco/10/GRCh38#16832862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#13286248-A-C

16832952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13286313-G-T

16833010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13286368-G-C

16833037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13286395-A-G

16833240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13286588-C-T

16833284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13286630-C-T

16833410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13286742-G-A

16833593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13286914-C-T

16834872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13287587-A-G

16835004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13287706-T-C

16835212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13287916-G-A

16835212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13287916-G-T

16835274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13287973-A-T

16835323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288020-G-A

16835323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288020-G-C

16835323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288020-G-T

16835331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288026-T-C

16835331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288026-T-G

16835358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288081-A-T

16835375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288098-A-G

16835480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288237-A-G

16835494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288251-G-A

16835627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288398-G-A

16835627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288398-G-T

16835653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288420-G-A

16835653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288420-G-T

16835713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288487-T-A

16836101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288680-G-A

16836101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288680-G-C

16836118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288697-T-C

16836217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13288775-T-A

16836353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13288910-A-G

16836462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13289017-A-G

16836593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13289126-A-T

16836957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13289448-G-C

16837057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13289550-C-G

16837091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13289585-G-T

16837289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13289781-A-T

16837530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13289897-C-G

16837913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13289993-T-G

16838096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13290175-G-A

16838288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13290357-G-A

16838485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13290529-A-G

16838576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13290604-C-T

16839014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13290746-C-T

http://identifiers.org/hco/10/GRCh38#16839041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13290773-C-A

16839181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13290909-C-T

16840248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13291734-A-G

16840303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13291766-G-C

16840303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13291766-G-T

16840334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13291796-G-A

16840355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13291817-T-C

16840362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: stop gained
orthologous variants: 13291824-G-A

16840402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13291864-T-A

16840412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13291874-T-G

16840482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13291944-G-A

16840482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13291944-G-T

16840501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13291963-G-A

16840522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13291984-T-C

16840548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13292010-G-A

16840548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13292010-G-T

16840588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13292048-C-T

http://identifiers.org/hco/10/GRCh38#16840596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13292056-C-A

16840759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13292234-T-A

16840759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13292234-T-C

http://identifiers.org/hco/10/GRCh38#16840853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13292334-C-A

16840853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13292334-C-T

16841007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13292478-G-A

16841007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13292478-G-C

16841007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13292478-G-T

http://identifiers.org/hco/10/GRCh38#16841088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13292559-A-C

16841158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13292648-T-C

16842649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13294875-C-T

16842668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13294894-T-A

16842805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13295001-G-C

16843173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13295297-T-G

16843241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13295365-A-G

16843336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13295502-G-A

16843359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13295528-C-G

16843359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13295528-C-T

16843441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13295581-A-G

16843483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13295617-T-C

16843939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13296044-G-A

16849075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13298308-A-G

16849143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13298377-T-C

16849282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13298510-G-A

16849317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13298544-A-T

16850959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13298780-C-T

16851173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13298963-G-A

16851174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13298964-G-A

16851174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13298964-G-T

16851184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13298974-T-C

16851203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13298982-T-C

http://identifiers.org/hco/10/GRCh38#16851207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13298986-C-A

http://identifiers.org/hco/10/GRCh38#16851373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13299147-C-A

16851373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13299147-C-T

16851438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 13299212-G-A

16851488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13299261-A-T

16851506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13299278-A-G

16851515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13299287-A-G

16851515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13299287-A-T

16852591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13299438-C-T

16852592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13299439-G-A

16852741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13299591-G-A

16853124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13299976-G-A

16855689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13301574-C-T

16855859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13301776-G-T

16855896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13301813-T-C

16856064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13302001-T-C

16856132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13302046-T-C

16856270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13302235-C-T

16856291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13302257-A-G

16856530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13302489-C-T

16856944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13302801-G-A

http://identifiers.org/hco/10/GRCh38#16857009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13302864-C-A

16862454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13307183-G-C

16862458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13307187-C-G

16862595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13307301-G-A

16862596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13307302-T-G

16862603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13307314-A-G

16862606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13307318-A-G

16862700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13307403-A-T

http://identifiers.org/hco/10/GRCh38#16862769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13307464-C-A

16863008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13307709-G-C

http://identifiers.org/hco/10/GRCh38#16865315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13308322-C-A

16865444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13308450-C-T

16865457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13308463-T-C

http://identifiers.org/hco/10/GRCh38#16866676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13308640-C-A

16866676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13308640-C-T

16866679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13308643-T-C

16866824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13308772-G-A

http://identifiers.org/hco/10/GRCh38#16867345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13309272-A-C

16867544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13309432-G-A

16868274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13309779-T-C

http://identifiers.org/hco/10/GRCh38#16868458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13310216-A-C

16868462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13310220-T-C

16868481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13310239-G-A

16868693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13310404-A-G

16868750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13310462-C-T

16868772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13310496-C-T

http://identifiers.org/hco/10/GRCh38#16868781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13310503-A-C

16868781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13310503-A-G

16868882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13310604-T-C

16868939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13310658-A-G

http://identifiers.org/hco/10/GRCh38#16869542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13310986-A-C

16869542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13310986-A-T

16869549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13310993-G-T

16869612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13311046-G-T

16869625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13311059-A-G

16869675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13311109-T-C

16869781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13311215-A-T

16869847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13311281-A-G

16869864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13311298-T-C

http://identifiers.org/hco/10/GRCh38#16869865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13311299-A-C

16869865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13311299-A-G

16869911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13311342-G-A

16869911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13311342-G-T

16869953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13311381-G-A

16869953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13311381-G-T

16869979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13311407-T-A

16869979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13311407-T-C

16869979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13311407-T-G

16869997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13311425-A-G

16870156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13311559-G-A

16873212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13312192-T-A

16873254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13312256-G-C

16873254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13312256-G-T

16873262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13312264-C-T

16873330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13312331-G-A

16873333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13312334-G-A

16873359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13312355-C-G

16873359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13312355-C-T

16873856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13312871-T-C

16874162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13313131-T-C

16874316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13313266-C-T

16874320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13313270-T-G

16874362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13313321-T-A

16874362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13313321-T-C

16874403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13313362-G-A

16874403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13313362-G-T

16874506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 13313465-G-A

16874533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13313488-G-A

16874586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13313541-T-G

16874720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13313648-G-A

16875166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13313881-C-G

16875326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13314029-T-A

16875392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13314085-T-C

16875431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13314117-C-T

16875473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13314159-A-T

16875746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13314415-C-T

16875776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13314439-T-C

16876181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13314821-A-G

16876887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13315316-G-A

16877040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13315469-T-C

16877194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13315591-A-T

16877226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13315635-A-G

16877233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13315642-T-A

16877233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13315642-T-C

http://identifiers.org/hco/10/GRCh38#16877345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13315745-C-A

16877451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13315853-G-A

16881117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13316622-A-T

16887249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13317519-A-G

http://identifiers.org/hco/10/GRCh38#16887348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13317618-C-A

16887406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13317719-C-T

http://identifiers.org/hco/10/GRCh38#16887733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13318166-A-C

16887998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13318419-C-G

http://identifiers.org/hco/10/GRCh38#16888316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13318686-C-A

16888316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13318686-C-T

16888351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13318726-G-A

16888351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13318726-G-T

16888359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13318738-T-C

16888544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13318920-G-T

http://identifiers.org/hco/10/GRCh38#16888586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13318961-C-A

16888586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13318961-C-T

16888604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13318983-T-C

16888604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13318983-T-G

http://identifiers.org/hco/10/GRCh38#16888640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13319015-C-A

16888674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13319046-G-A

16888674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13319046-G-T

16888692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13319062-G-A

16888692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13319062-G-C

16890412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13319505-T-C

http://identifiers.org/hco/10/GRCh38#16890470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13319563-C-A

16890470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13319563-C-T

16890497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13319590-C-T

16890510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13319603-C-T

http://identifiers.org/hco/10/GRCh38#16890544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13319636-C-A

16890544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13319636-C-T

16890635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13319720-A-G

16890639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13319724-G-A

16890639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13319724-G-T

16890680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13319755-A-G

16897504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13321436-C-T

16897958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13321855-T-G

16898096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13321971-C-T

16898471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13322314-C-G

16898839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13322821-G-A

16898914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13322894-A-G

16898914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13322894-A-T

16898934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13322917-A-G

16898934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13322917-A-T

16899162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13323134-G-A

16899171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13323143-A-G

16899280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13323254-T-A

16899280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13323254-T-C

16899311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13323286-T-C

16899311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13323286-T-G

16899353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13323323-T-C

16899484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13323448-A-G

http://identifiers.org/hco/10/GRCh38#16899487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13323451-C-A

http://identifiers.org/hco/10/GRCh38#16899596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13323564-C-A

http://identifiers.org/hco/10/GRCh38#16899633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13323613-C-A

16899678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13323658-G-T

16899692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13323672-A-G

16899835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13323850-T-G

16900012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13324017-C-G

http://identifiers.org/hco/10/GRCh38#16900107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13324117-C-A

16900594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13324562-G-C

16900806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13324782-A-G

16900901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13324869-C-G

16900901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13324869-C-T

16900922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13324953-T-A

16900922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13324953-T-C

16900984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13325013-C-G

16900984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13325013-C-T

16901084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13325127-C-T

16901098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13325141-G-A

16901197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13325232-G-T

16901224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13325257-A-G

16901224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13325257-A-T

16901344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13325986-G-T

http://identifiers.org/hco/10/GRCh38#16901374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13326016-A-C

16901565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13326199-A-G

16901565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13326199-A-T

16902529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13326608-T-C

16902790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13326874-G-A

16902800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13326884-T-G

http://identifiers.org/hco/10/GRCh38#16903012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13327040-C-A

16903074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13327105-T-C

16903074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13327105-T-G

http://identifiers.org/hco/10/GRCh38#16903098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13327138-A-C

16903335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13327348-T-G

16903449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13327474-T-C

16903497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13327543-C-T

16903509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13327555-A-G

16903510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13327556-G-A

16904246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13328044-G-A

16904246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13328044-G-T

16905175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13328955-A-G

16905305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13329399-T-C

http://identifiers.org/hco/10/GRCh38#16905390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13329499-C-A

16905390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13329499-C-G

16905390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13329499-C-T

http://identifiers.org/hco/10/GRCh38#16905462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13329570-A-C

16905523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13329630-C-G

16905614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13329733-G-A

16905614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13329733-G-T

16905651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13329762-C-T

16905764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13329875-T-C

16906166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13329931-A-T

16906167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13329932-G-A

16906167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13329932-G-T

16906216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13329981-G-A

16906249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13330014-T-C

16906344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13330109-T-C

16906430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13330192-A-G

16906439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13330200-A-G

16906443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13330204-G-A

16906443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13330204-G-C

16906443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13330204-G-T

http://identifiers.org/hco/10/GRCh38#16906478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13330239-A-C

16906484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13330245-A-G

16906517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13330273-T-C

16906559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13330309-G-A

16906816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13330562-T-C

16906946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13330659-T-C

16907024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13330731-A-G

16907184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13330888-T-C

16907222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13330922-G-A

16907278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13330980-C-T

16907318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13331225-T-C

16907362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13331277-C-G

16907431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13331390-G-A

16907431-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13331390-G-C

16907431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13331390-G-T

http://identifiers.org/hco/10/GRCh38#16907437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13331396-A-C

16907463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13331422-G-C

16907463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13331422-G-T

16907707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13331666-G-C

16907707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13331666-G-T

16907738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13331697-G-A

16907738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13331697-G-C

16907738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13331697-G-T

16907759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13331719-G-C

16907759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13331719-G-T

http://identifiers.org/hco/10/GRCh38#16907807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13331755-A-C

16908496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13332749-C-T

16908547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13332800-C-T

16909269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13333420-G-A

16909289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13333439-T-C

16909296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13333446-T-C

http://identifiers.org/hco/10/GRCh38#16909805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13333912-A-C

16909909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13334019-G-A

16910303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13334149-C-T

16910500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13334324-C-T

16910501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13334325-A-G

16910568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13334418-C-T

16910806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13334594-T-C

16911340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13335050-C-T

16911504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13335219-T-C

16912254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13335494-A-G

16912402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13335627-T-C

http://identifiers.org/hco/10/GRCh38#16912536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13335697-C-A

16912584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13335748-G-A

16912584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13335748-G-C

16913569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13336074-C-T

16913689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13336177-T-G

16913695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13336183-G-T

http://identifiers.org/hco/10/GRCh38#16913779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13336261-A-C

16913813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 13336294-T-A

16913813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 13336294-T-C

16913835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13336316-C-G

16913835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13336316-C-T

16913889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13336370-C-T

16913893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13336374-G-A

16913893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13336374-G-T

16913928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13336409-A-G

16913992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 13336473-T-G

16914086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13336540-T-A

16914145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13336598-T-C

16914779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13336853-G-A

16914783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13336873-T-A

16914794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13336884-G-A

16914794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13336884-G-C

http://identifiers.org/hco/10/GRCh38#16914893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13336973-C-A

16914955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13337047-T-C

http://identifiers.org/hco/10/GRCh38#16915037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13337129-A-C

16915037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13337129-A-G

16915175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 13337267-G-T

16915225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13337320-C-G

16915225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13337320-C-T

16915264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13337363-T-A

16915264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13337363-T-C

http://identifiers.org/hco/10/GRCh38#16915276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13337375-C-A

16915283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13337382-T-C

16915396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13337488-A-G

http://identifiers.org/hco/10/GRCh38#16915571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13337645-C-A

16915735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13337812-C-T

16915767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13337844-A-T

16916004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13338340-G-T

16916034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 13338370-C-T

16916084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13338402-T-C

16916150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13338466-T-C

http://identifiers.org/hco/10/GRCh38#16916158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13338474-A-C

16916169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13338485-T-A

16916251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13338564-A-T

16916337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13338650-A-G

16916537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13338858-A-G

16916754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13339095-T-C

16917632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13339305-T-A

16918613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13339572-A-G

16918615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 13339579-T-A

16918714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13339678-C-T

16918786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13339750-T-C

16918922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13339886-G-A

16918922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13339886-G-T

16919062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13340014-T-C

16919261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13340171-G-A

16919432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13340360-C-T

http://identifiers.org/hco/10/GRCh38#16919587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13340520-C-A

16919725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13340658-G-A

16919729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13340662-C-T

16919765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13340694-A-G

http://identifiers.org/hco/10/GRCh38#16919830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13340758-C-A

16919830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13340758-C-T

http://identifiers.org/hco/10/GRCh38#16919831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13340759-C-A

16919848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13340775-T-C

16919937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13340873-A-G

16920007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13340943-T-A

16920007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13340943-T-C

16920007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13340943-T-G

http://identifiers.org/hco/10/GRCh38#16920049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13340985-A-C

16920091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13341027-A-G

16920153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13341087-C-T

16920195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13341126-G-A

16920195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13341126-G-T

16920211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13341137-T-A

http://identifiers.org/hco/10/GRCh38#16920219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13341145-A-C

http://identifiers.org/hco/10/GRCh38#16920280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13341207-C-A

16920308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13341236-G-C

16920315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13341243-G-A

16923364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13343065-C-T

16923582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13343238-G-C

16923582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13343238-G-T

16923735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13343360-A-G

16923838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13343451-A-G

16924588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13343991-G-T

http://identifiers.org/hco/10/GRCh38#16925072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13344454-C-A

16925089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13344470-A-G

16925090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13344471-T-C

16925090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13344471-T-G

16925108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13344488-A-G

16925218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13344611-T-C

16925392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13344785-G-C

16925567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13344935-G-A

http://identifiers.org/hco/10/GRCh38#16925653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13345022-A-C

16925653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13345022-A-G

16925800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345169-T-C

16925800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345169-T-G

16925816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345185-G-T

16925829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345198-T-G

16925901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345266-T-A

16925901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345266-T-C

16925902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345267-G-A

16925902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345267-G-T

16925906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345271-G-A

16925906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345271-G-C

16925906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345271-G-T

16925911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345276-G-T

16925925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345290-G-A

16925925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345290-G-T

16926049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345405-C-T

16926134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345479-T-C

16926204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345537-G-C

16926270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13345603-G-A

16927341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13346193-G-A

16927363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13346215-G-T

16927370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13346222-T-C

16927818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13346680-A-G

16927915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13346775-G-A

16928048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13346894-C-T

16928052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13346900-T-C

16928173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13347262-A-G

16928239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13347328-C-T

16928240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13347329-C-T

16928256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13347345-T-G

16928328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13347420-A-T

16928375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13347468-C-G

16928410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13347503-G-C

16928410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13347503-G-T

16928438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13347531-A-G

16928438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13347531-A-T

http://identifiers.org/hco/10/GRCh38#16928446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13347539-A-C

16928481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13347572-G-A

16929367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13348027-C-T

16929384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13348043-G-A

16929641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13348289-G-C

16929908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13349614-A-G

16930008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13349712-G-C

http://identifiers.org/hco/10/GRCh38#16930074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13349764-C-A

16930074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13349764-C-G

16930185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13349860-C-G

http://identifiers.org/hco/10/GRCh38#16930378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13350015-A-C

16930399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13350036-T-C

16930467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13350098-C-T

16930844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13350661-A-G

16931772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13351267-G-C

16931772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13351267-G-T

16931841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13351337-A-G

16932129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13351574-A-G

16932150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13351593-T-G

16932373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13351812-G-A

16933184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13352431-G-A

16933205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13352452-A-G

16933303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13352550-C-G

16933303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13352550-C-T

16937807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13353028-G-C

16937807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13353028-G-T

16937813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13353034-T-C

16937818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13353040-T-G

http://identifiers.org/hco/10/GRCh38#16937864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13353092-A-C

16937864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13353092-A-G

http://identifiers.org/hco/10/GRCh38#16937901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13353124-A-C

16937938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13353158-G-T

16938048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13353260-G-A

16938088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13353297-G-A

16938528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13353605-T-C

16938537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13353614-G-A

16938650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13353732-T-C

16938787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13354497-T-C

16938822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13354532-G-C

16938822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13354532-G-T

16938853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13354555-A-G

16938968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13354667-A-G

16939038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13354737-T-C

16939038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13354737-T-G

16939107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13354806-G-A

16939152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 13354851-G-A

16939218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13354936-A-G

16939238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13354962-G-T

16939278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13355002-G-C

16939373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13355115-C-T

16940042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13355693-T-A

16940042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13355693-T-C

16940065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13355716-T-G

16940111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13355762-G-A

16940237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 13355888-T-C

http://identifiers.org/hco/10/GRCh38#16940262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13355915-A-C

16943555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13356202-A-T

16943690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13356340-C-T

16943910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13356947-G-A

16943910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13356947-G-C

16944076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13357096-T-C

http://identifiers.org/hco/10/GRCh38#16944387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13357195-C-A

16944387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13357195-C-T

16944665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13357476-C-T

16944872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13357997-G-T

16944919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13358042-T-C

16945161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13358755-A-G

16945180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13358774-G-A

16945256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13358848-G-A

16945291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13358882-G-A

16945854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13359116-G-A

16946198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13359550-T-A

http://identifiers.org/hco/10/GRCh38#16946484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13359992-C-A

16947148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13360292-C-T

16947176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13360320-G-T

16947345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13360489-C-T

16947349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13360493-T-C

16947354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13360498-C-T

16947479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13360623-T-C

16947511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13360655-T-C

16947717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13360828-G-A

http://identifiers.org/hco/10/GRCh38#16947737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13360877-A-C

16947782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13360906-G-A

16948317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13361242-T-C

http://identifiers.org/hco/10/GRCh38#16948686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13361674-C-A

16948686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13361674-C-T

16949017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13361992-G-C

16949029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362004-T-C

16949173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362146-T-C

16949193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362168-A-T

http://identifiers.org/hco/10/GRCh38#16949252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13362232-A-C

16949332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362296-A-G

16949353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362312-C-G

16949544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362429-C-T

16949572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362457-G-A

16949603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362483-C-T

16949615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362488-C-T

16949617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362490-T-A

16949700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362567-A-G

16949817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362693-G-T

http://identifiers.org/hco/10/GRCh38#16949879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13362753-C-A

16949939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362812-T-A

16949939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362812-T-C

16949948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362821-A-G

16949987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362916-G-A

16949987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13362916-G-T

16950027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13362956-C-T

16950066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13362995-C-T

http://identifiers.org/hco/10/GRCh38#16950151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13363092-C-A

16950151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13363092-C-T

16950800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13363369-T-C

16950822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13363415-C-T

16950910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13363484-T-C

16950930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13363503-T-C

16950970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13363543-T-G

16951159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13363735-G-A

16951234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13363786-G-C

16951303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13363860-T-C

16951477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13364010-T-C

http://identifiers.org/hco/10/GRCh38#16951486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13364019-A-C

16951666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13364183-A-G

http://identifiers.org/hco/10/GRCh38#16951769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13364294-C-A

16951808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13364339-G-A

16951878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13364406-C-T

http://identifiers.org/hco/10/GRCh38#16952136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13364862-A-C

16952136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13364862-A-G

16952423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13365209-T-C

16952448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13365234-A-G

16952478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13365266-A-G

16952686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13365452-C-T

16953077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13365821-G-A

16953312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13366052-C-T

16953365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13366098-G-T

16953377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13366109-C-G

16953384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13366116-C-T

16953415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13366148-T-A

16953516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13366268-G-A

16953914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13366613-A-G

16954249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13366911-G-T

16954399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13367024-T-C

16954580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13367210-T-A

16954580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13367210-T-G

http://identifiers.org/hco/10/GRCh38#16954662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13367290-C-A

16954662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13367290-C-G

16954674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13367308-G-A

16954674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13367308-G-T

http://identifiers.org/hco/10/GRCh38#16954675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13367309-C-A

http://identifiers.org/hco/10/GRCh38#16955417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13367512-C-A

16955691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13367784-T-C

http://identifiers.org/hco/10/GRCh38#16956013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13368031-C-A

16956158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13368141-T-A

16956158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13368141-T-C

16956255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13368239-T-G

http://identifiers.org/hco/10/GRCh38#16959916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13371921-C-A

16959916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13371921-C-T

16960600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13372249-T-C

16960712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13372341-T-C

16960792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13372435-G-C

16960833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13372478-A-G

http://identifiers.org/hco/10/GRCh38#16960843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13372488-C-A

16960931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13372576-C-T

16960946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13372590-C-T

16960962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13372605-G-C

16960964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13372607-G-T

16961035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13372678-G-T

16961420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13372754-T-C

16961446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13372779-A-G

http://identifiers.org/hco/10/GRCh38#16961595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13372926-C-A

16961595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13372926-C-G

http://identifiers.org/hco/10/GRCh38#16965253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13373460-A-C

16965253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13373460-A-G

16965271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13373480-T-G

16965278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13373487-C-T

http://identifiers.org/hco/10/GRCh38#16965329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13373530-A-C

16965401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13373606-A-T

16965444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13373649-C-T

16965488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13373693-G-A

16965527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13373740-A-G

16965542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13373757-G-A

16965542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13373757-G-T

http://identifiers.org/hco/10/GRCh38#16965727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13374253-C-A

16965727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13374253-C-G

16965727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13374253-C-T

16965771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13374294-A-G

16965869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13374389-G-A

16965869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 13374389-G-T

16965950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 13374471-T-C

16966051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13374569-T-C

16966105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13374699-G-T

http://identifiers.org/hco/10/GRCh38#16966238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#13374983-A-C

16966239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13374984-T-C

16966250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13374995-G-A

16966250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13374995-G-C

16966341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13375085-G-T

16966345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13375089-C-T

16966368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13375113-G-A

16966368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13375113-G-T

http://identifiers.org/hco/10/GRCh38#16966403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#13375151-C-A

16966561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13375333-G-T

16966622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13375475-T-C

16966652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13375538-T-A

16966657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13375543-C-T

16966676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13375565-T-G

16966724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13375656-C-T

16967264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13376244-T-C

16967443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13376371-T-C

http://identifiers.org/hco/10/GRCh38#16967526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13376432-A-C

16968152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13376708-C-G

16968345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13376906-A-T

16968434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13377071-C-T

16968485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 13377124-T-C

16969990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13380254-G-C

http://identifiers.org/hco/10/GRCh38#16970031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13380283-C-A

16970031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13380283-C-T

16970084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13380328-G-T

16970122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13380366-G-A

http://identifiers.org/hco/10/GRCh38#16970174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13380464-C-A

16970829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13380678-T-C

16971071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13380858-C-T

16971178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13380964-G-A

16971688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13381460-A-G

16971688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13381460-A-T

16971874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13382090-T-C

16971879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13382095-C-T

16972158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13382301-C-T

16972233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13382358-A-G

16972798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13382848-T-C

16972922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13382967-C-T

16973127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13383120-G-T

http://identifiers.org/hco/10/GRCh38#16973222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13383213-C-A

16973256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13383238-T-G

16973350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13383327-A-G

16973391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13383368-G-C

16973391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13383368-G-T

16973454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13383428-T-C

16973993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13383472-T-A

16974105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13383584-G-C

16974126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13383605-A-G

16975163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13383905-G-A

16975201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13383937-C-T

16975278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13384012-A-G

16975278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13384012-A-T

16975279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13384013-C-T

16975302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13384041-A-G

16975413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13384157-A-G

http://identifiers.org/hco/10/GRCh38#16975453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13384198-C-A

16977962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13385153-T-G

16977964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13385155-G-A

16977964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13385155-G-C

16978091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13385279-G-A

16978317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13385496-T-C

16978413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13385566-G-A

16978461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13385625-A-G

16982055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386225-G-A

16982070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386232-A-G

16982118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386271-C-T

16982161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386320-T-G

16982314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386404-G-C

16982350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386466-G-A

16982350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386466-G-T

http://identifiers.org/hco/10/GRCh38#16982354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13386470-C-A

16982354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386470-C-G

16982354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386470-C-T

16982493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13386578-A-G

16982577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13386662-T-C

16982628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13386713-G-T

16982670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386755-C-T

16982682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386767-G-C

16982682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386767-G-T

16982683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386768-A-G

16982709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386800-A-G

16982721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386812-G-C

16982721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386812-G-T

16982734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386825-A-G

http://identifiers.org/hco/10/GRCh38#16982737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13386828-C-A

16982737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386828-C-T

http://identifiers.org/hco/10/GRCh38#16982802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13386893-C-A

16982840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13386927-G-A

16983055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13387331-A-G

16983166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13387418-C-T

16983333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13387542-T-C

16983373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13387577-C-G

16983373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13387577-C-T

16983418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13387619-T-C

16983440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13387641-T-G

16983460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13387660-G-T

16983493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13387693-C-G

http://identifiers.org/hco/10/GRCh38#16983502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13387702-C-A

16984006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13388580-G-C

16984006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13388580-G-T

http://identifiers.org/hco/10/GRCh38#16984021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13388595-C-A

16984058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13388632-C-T

http://identifiers.org/hco/10/GRCh38#16984091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13388667-C-A

16984094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13388670-T-C

16984119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13388695-T-C

16984193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13388769-G-T

16984265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13388841-G-A

16984265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13388841-G-C

16984284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 13388860-C-T

16984317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13388909-T-C

16984319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13388911-T-G

16984414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13389001-G-A

16984414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13389001-G-C

16984414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13389001-G-T

16984419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13389006-G-A

16984419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13389006-G-T

http://identifiers.org/hco/10/GRCh38#16984428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13389015-A-C

16984480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13389067-C-G

16984585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13389158-G-T

16984718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13389240-T-A

http://identifiers.org/hco/10/GRCh38#16984756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13389280-A-C

16985896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13389603-C-T

http://identifiers.org/hco/10/GRCh38#16986126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13389775-C-A

16986205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13389827-C-G

16986205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13389827-C-T

16986391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13389990-G-A

16986391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13389990-G-C

http://identifiers.org/hco/10/GRCh38#16986473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13390100-C-A

http://identifiers.org/hco/10/GRCh38#16986617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13390251-C-A

16986617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13390251-C-T

16986730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13390317-C-T

16986938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13390516-A-G

16987103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13390682-C-T

16987489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13391058-G-C

http://identifiers.org/hco/10/GRCh38#16987541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#13391098-A-C

16987541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13391098-A-G

16987615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13391172-T-A

16987621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13391187-G-A

16987657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13391231-G-C

16987767-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13391366-T-G

http://identifiers.org/hco/10/GRCh38#16988273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13391837-A-C

16988288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13391852-C-T

http://identifiers.org/hco/10/GRCh38#16988320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13391883-C-A

16988320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13391883-C-T

16988326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13391889-G-T

16988381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13391947-G-A

16988417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13392000-C-T

16988840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13392620-G-A

16988929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13392705-G-A

16988996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13392766-G-A

16989066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13392831-C-G

http://identifiers.org/hco/10/GRCh38#16989962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13393315-C-A

16989982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13393335-C-T

16990157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13393479-C-T

16990191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13393515-G-T

http://identifiers.org/hco/10/GRCh38#16990243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13393571-A-C

16990243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13393571-A-T

16990254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13393582-G-A

16990254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13393582-G-T

16990282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13393599-C-T

16990436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous_variant, undefined
orthologous variants: 13393752-C-T

16990552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13393866-G-A

16990552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13393866-G-T

16990583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13393897-A-G

http://identifiers.org/hco/10/GRCh38#16990584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13393898-A-C

16990584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13393898-A-G

http://identifiers.org/hco/10/GRCh38#16990587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13393901-C-A

16990617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13393926-T-A

16992830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13394721-T-G

16992886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13394777-G-A

http://identifiers.org/hco/10/GRCh38#16992899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13394790-A-C

http://identifiers.org/hco/10/GRCh38#16992948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13394840-A-C

16993003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13394894-G-A

16993008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13394899-C-T

16993031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13394926-T-C

16993047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13394943-C-T

16995797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13395598-T-C

16995821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13395622-T-G

16995859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13395638-T-G

16995949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13395704-G-A

16996098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13395827-A-G

16996102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13395831-T-C

16996253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13395984-A-G

16996364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13396092-C-G

16996385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13396112-T-C

http://identifiers.org/hco/10/GRCh38#16996739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13396399-C-A

16996739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13396399-C-T

16996785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13396453-T-G

16996799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13396466-A-G

16997432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13397032-T-A

16997573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13397158-C-G

16998051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13397351-T-A

16998182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13397487-C-T

16998562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13397828-C-T

16998769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398010-A-G

16998950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398151-T-C

16999173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398362-T-C

16999195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398384-T-G

16999227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398415-A-T

http://identifiers.org/hco/10/GRCh38#16999229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13398417-C-A

16999258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398446-A-G

16999333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398506-T-C

16999376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398550-C-G

16999376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398550-C-T

http://identifiers.org/hco/10/GRCh38#16999394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13398566-A-C

16999394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398566-A-T

16999460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398644-C-G

16999474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398658-T-C

16999474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398658-T-G

16999475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398659-G-A

16999503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398687-A-G

16999518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398712-T-C

16999532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398739-G-A

16999534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398741-T-G

16999598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13398802-G-A

16999796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13399000-A-G

16999907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13399109-G-C

http://identifiers.org/hco/10/GRCh38#17000074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13399392-C-A

17000212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13399522-A-G

17000357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13399740-G-A

17000375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13399755-G-A

17000433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13399814-G-A

17000433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13399814-G-T

17000642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13400045-A-G

17000656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13400056-G-A

17000684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13400084-C-T

17000731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13400128-T-G

17000748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13400145-T-C

17000796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13400192-G-C

17001662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13400339-A-G

17001679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13400356-A-G

17001681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13400358-G-A

17001713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13400395-C-T

17001735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13400417-T-C

17002077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13400846-T-C

http://identifiers.org/hco/10/GRCh38#17002121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13400856-A-C

17002121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13400856-A-G

17002127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13400862-G-A

17002356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13401056-G-T

17002475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13401176-C-T

17002582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13401287-C-G

17002582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13401287-C-T

17002708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13401431-G-A

http://identifiers.org/hco/10/GRCh38#17002728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13401449-C-A

17002728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13401449-C-T

17002946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13401786-C-T

17003092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13401928-C-T

17003285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13402193-A-G

17003359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13402255-G-A

17003363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13402259-T-G

http://identifiers.org/hco/10/GRCh38#17003427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#13402317-C-A

17003449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13402339-G-A

17003472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13402346-C-T

17003616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13402426-T-C

17003668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13402471-T-C

17003709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13402499-C-T

http://identifiers.org/hco/10/GRCh38#17003712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13402502-C-A

http://identifiers.org/hco/10/GRCh38#17006553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13403506-A-C

17006626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13403557-C-T

http://identifiers.org/hco/10/GRCh38#17006630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13403561-C-A

17006682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13403604-G-A

17006696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13403618-G-A

17006791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13403710-T-C

http://identifiers.org/hco/10/GRCh38#17006853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13403776-C-A

17006853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13403776-C-G

17006974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13403897-C-T

17006989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13403913-C-T

17007080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13404003-G-A

17007145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13404066-C-T

http://identifiers.org/hco/10/GRCh38#17007149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13404070-C-A

17007149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13404070-C-T

17007226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13404124-T-G

17007231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13404129-C-T

17007298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13404203-T-C

17008586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405005-C-T

17008588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405007-G-A

17008588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405007-G-T

http://identifiers.org/hco/10/GRCh38#17008681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13405086-C-A

17008681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405086-C-T

17008737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405139-C-T

17008748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405150-A-G

17008795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405185-G-T

17008999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405357-T-A

17008999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405357-T-C

17009021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405388-G-A

17009261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405614-G-A

http://identifiers.org/hco/10/GRCh38#17009392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#13405754-A-C

17009455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405816-C-T

17009462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405827-T-C

17009464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405829-C-G

17009464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405829-C-T

17009551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13405906-G-A

17009625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13405987-G-A

17009764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13406102-G-C

17009849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13406179-T-C

http://identifiers.org/hco/10/GRCh38#17009997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13406328-C-A

17010048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13406379-G-A

17010137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13406569-T-A

17010264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13406700-G-A

17010287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13406723-A-G

17010295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13406731-G-C

17010295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13406731-G-T

http://identifiers.org/hco/10/GRCh38#17019083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13408072-A-C

http://identifiers.org/hco/10/GRCh38#17019127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13408111-A-C

17019264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13408242-C-G

17019267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13408245-C-T

17019318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13408296-C-G

17019322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13408300-T-A

17019481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13408465-T-C

17019687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13408631-A-G

17019687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13408631-A-T

17019697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13408641-T-C

http://identifiers.org/hco/10/GRCh38#17019721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13408665-C-A

17019721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13408665-C-G

http://identifiers.org/hco/10/GRCh38#17019780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13408724-A-C

17019786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13408730-G-T

17019801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13408745-G-T

17019811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13408755-C-T

17020022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13408970-G-C

17020027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13408975-G-A

17021919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13410049-C-T

17022271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13410378-G-C

http://identifiers.org/hco/10/GRCh38#17022529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13411182-A-C

17022600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411253-G-A

17022822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411517-G-A

17022929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411585-T-G

17022938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411594-A-G

17022966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411625-C-T

17023035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411699-A-G

17023072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411740-G-A

17023147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411810-T-A

17023147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411810-T-C

17023186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411841-A-G

http://identifiers.org/hco/10/GRCh38#17023192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13411848-A-C

17023192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411848-A-G

17023199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411855-G-C

17023283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411938-T-G

17023324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411979-G-A

17023324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411979-G-C

17023336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411991-T-A

http://identifiers.org/hco/10/GRCh38#17023339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13411994-C-A

17023339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13411994-C-T

17023460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13412143-G-A

17023460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13412143-G-T

http://identifiers.org/hco/10/GRCh38#17023705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13412408-C-A

17023706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13412409-A-G

17023725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13412423-G-A

17023725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13412423-G-C

17023725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13412423-G-T

17023734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13412428-A-G

http://identifiers.org/hco/10/GRCh38#17024039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13412714-C-A

http://identifiers.org/hco/10/GRCh38#17024239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13412926-A-C

17024258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13412943-T-C

17025357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13414429-T-C

17025579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13414593-C-G

17025681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13414700-C-G

17025697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 13414716-A-G

17026861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13415608-T-C

17026872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13415619-G-C

17026872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13415619-G-T

17027072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13415853-G-A

17027688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13416444-C-T

17027700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13416456-T-C

17027746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13416494-C-T

17028051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13416659-T-C

17028143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13416751-C-T

17028156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13416764-A-G

http://identifiers.org/hco/10/GRCh38#17028400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13416965-A-C

17028400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13416965-A-G

17028401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13416966-G-A

17028942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13417408-T-C

http://identifiers.org/hco/10/GRCh38#17029193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13417729-A-C

17029207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13417739-T-G

17029223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13417755-G-A

17029239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13417771-C-T

17029271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13417798-T-G

17029406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13418229-T-G

17029497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13418304-G-A

17029529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13418335-A-G

17029902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13418709-T-C

http://identifiers.org/hco/10/GRCh38#17031001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13419608-A-C

17031084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13419686-C-T

17031143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13419743-C-G

17031143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13419743-C-T

17031168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13419768-T-G

17031314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13419902-A-G

17031319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13419906-T-G

17031520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13420096-T-C

17031520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13420096-T-G

17031560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13420136-C-T

17031658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13420222-G-A

http://identifiers.org/hco/10/GRCh38#17031698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13420272-C-A

17031752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13420331-T-C

17031796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13420377-G-A

17031796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13420377-G-T

17031818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13420399-C-T

17031896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13420472-A-G

17032166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13420754-A-T

17032179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13420767-G-A

http://identifiers.org/hco/10/GRCh38#17033208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13421315-C-A

17033270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13421364-C-T

17033293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13421387-A-G

17033363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13421462-C-T

17033364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13421463-G-A

17033442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13421537-C-G

17033486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13421579-C-T

17033495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13421588-G-A

17033517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13421594-A-G

17033901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13421917-G-T

17035107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13423977-G-A

http://identifiers.org/hco/10/GRCh38#17035108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13423978-C-A

17035361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13424199-T-C

17035619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13424357-G-A

17035694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13424414-T-C

17036153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13424736-T-C

17036183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13424766-G-A

17036371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13424898-C-T

17036766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13425166-G-C

17036785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13425183-G-A

17036853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13425251-C-T

17036950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13425329-G-A

17036950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13425329-G-C

17036964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13425343-C-T

17037187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13425550-T-A

17037411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13425765-T-C

17037501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13425873-C-T

17037834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13426170-T-G

http://identifiers.org/hco/10/GRCh38#17037851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13426184-C-A

17037870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13426201-G-T

17038181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13426366-T-C

17038231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13426393-T-C

17038750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13426889-G-A

17038870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427007-C-T

17039087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427244-C-G

17039124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427273-G-A

17039140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427289-G-A

17039151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427300-T-C

17039162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427311-C-T

17039170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427319-G-A

17039170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427319-G-T

17039179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427328-G-A

17039179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427328-G-C

17039180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427329-C-T

17039197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427354-C-T

17039205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427362-G-A

17039262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427415-G-A

17039355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427507-G-A

17039371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427519-C-G

17039418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13427565-C-G

17039829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13428082-G-A

http://identifiers.org/hco/10/GRCh38#17039899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13428286-A-C

17040065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13428444-A-G

17040110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13428487-G-A

17040116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13428494-G-A

17040130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13428508-G-C

17040133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13428511-T-C

17040506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429065-A-T

17040522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429081-A-G

17040914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429363-T-G

17040928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429377-G-T

17040931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429380-G-A

17040931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429380-G-T

17040940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429389-G-T

17040942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429391-G-T

17040949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429398-T-C

17040949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429398-T-G

17040966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429415-G-T

17041007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429457-G-T

17041012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429462-A-T

http://identifiers.org/hco/10/GRCh38#17041099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13429549-A-C

17041099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13429549-A-G

17041130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13429580-T-C

17041314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429761-T-C

17041335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429775-A-G

17041335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429775-A-T

http://identifiers.org/hco/10/GRCh38#17041371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13429811-C-A

17041371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13429811-C-G

17041636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13430031-G-A

17041671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13430066-T-C

17042172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13430563-T-G

17043321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13431363-T-C

17043600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13431617-C-T

17043682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13431701-A-G

17043682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13431701-A-T

17043695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13431714-A-G

http://identifiers.org/hco/10/GRCh38#17043718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13431718-C-A

17043718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13431718-C-T

http://identifiers.org/hco/10/GRCh38#17043910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13431846-C-A

17043910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13431846-C-T

17043955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13431891-T-G

http://identifiers.org/hco/10/GRCh38#17044003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13431939-A-C

17044006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13431942-T-C

17044058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13431984-T-A

17044058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13431984-T-G

17044077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432003-A-G

http://identifiers.org/hco/10/GRCh38#17044225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13432008-C-A

17044225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432008-C-T

http://identifiers.org/hco/10/GRCh38#17044229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13432012-A-C

17044648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432282-A-G

17044669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432302-A-G

17044750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432383-T-C

17044806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432439-T-C

17044808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432441-C-T

17044870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432509-T-C

17044873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432512-T-C

17044876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432515-T-A

17044899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432539-G-A

17044899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432539-G-T

17044909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432549-G-T

http://identifiers.org/hco/10/GRCh38#17044933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13432573-A-C

17044957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432600-G-A

17044957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432600-G-C

17044957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432600-G-T

17045046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13432687-G-A

http://identifiers.org/hco/10/GRCh38#17045098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13432739-C-A

17045098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13432739-C-G

17045148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13432789-T-A

17045148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13432789-T-C

17045148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13432789-T-G

17045215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432855-C-T

17045258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432893-T-C

http://identifiers.org/hco/10/GRCh38#17045281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13432916-C-A

17045281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432916-C-T

17045284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432919-T-C

http://identifiers.org/hco/10/GRCh38#17045290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13432925-C-A

17045290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432925-C-G

17045291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13432926-A-G

17045885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13433369-A-T

http://identifiers.org/hco/10/GRCh38#17045888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13433372-C-A

17045888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13433372-C-T

17045983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13433468-T-C

17045984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13433469-T-C

17046243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13433711-A-G

17046288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13433776-A-G

http://identifiers.org/hco/10/GRCh38#17046434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13433913-C-A

17046503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13433974-A-T

17046533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13434004-G-C

17046701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13434315-C-T

17046715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13434329-T-A

http://identifiers.org/hco/10/GRCh38#17046808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13434425-C-A

17046844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13434461-G-A

17047066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13434659-G-A

17047671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13435873-A-G

17047811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13436004-G-C

17048001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13436188-G-C

17048096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13436290-G-C

17048380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13436580-C-T

17048700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13436728-T-C

17048831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13436846-T-C

17048992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13436965-C-G

17048992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13436965-C-T

17059301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13440070-C-T

17059641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13440530-C-T

17059880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13440748-G-C

17061512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13442247-T-C

17061572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13442301-C-G

17061608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13442337-A-T

17061870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13442515-T-C

17061891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13442536-A-G

17061949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13442594-G-A

17061985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13442630-T-C

17062070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13442699-G-A

17062073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13442704-C-G

17062073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13442704-C-T

17062122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13442752-T-C

17062320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13442874-T-A

http://identifiers.org/hco/10/GRCh38#17062425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13442980-A-C

17062524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13443061-G-A

17062686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13443226-G-A

17062712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13443252-A-G

http://identifiers.org/hco/10/GRCh38#17062806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13443343-C-A

17062842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13443378-T-C

http://identifiers.org/hco/10/GRCh38#17063047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#13443554-A-C

17063091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13443594-C-G

17063310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13443755-C-T

17063311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13443756-G-A

17063311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13443756-G-C

http://identifiers.org/hco/10/GRCh38#17063333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#13443770-C-A

17063452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13443886-C-T

http://identifiers.org/hco/10/GRCh38#17063499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13444018-C-A

17063641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13444153-C-T

17063740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13444263-T-C

17063856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13444379-G-A

17063856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13444379-G-T

http://identifiers.org/hco/10/GRCh38#17064035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13444552-C-A

17064050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13444567-G-A

17064050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13444567-G-C

17064125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13444641-C-T

http://identifiers.org/hco/10/GRCh38#17064205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13444719-A-C

17064205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13444719-A-G

17064257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13444761-T-A

17064257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13444761-T-C

17064445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13444944-G-A

http://identifiers.org/hco/10/GRCh38#17064524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13444969-C-A

17064551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13444997-T-C

17065468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13445211-T-A

17065468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13445211-T-C

http://identifiers.org/hco/10/GRCh38#17065617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13445335-C-A

17065617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13445335-C-T

17065620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13445338-G-A

17065649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13445367-C-G

17065677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13445403-G-A

http://identifiers.org/hco/10/GRCh38#17065692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13445417-A-C

http://identifiers.org/hco/10/GRCh38#17065758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13445482-C-A

17065758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13445482-C-T

17065950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13445643-A-G

17066096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13445799-T-A

17066319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13446024-T-C

17066489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13446157-G-A

17066502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13446170-G-T

17066567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13446239-T-C

http://identifiers.org/hco/10/GRCh38#17066607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13446265-C-A

17066716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13446376-A-G

17066916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13446920-C-G

17066991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13446990-T-A

17066991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13446990-T-C

17067152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13447149-A-T

http://identifiers.org/hco/10/GRCh38#17067272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13447268-C-A

17067281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13447277-A-T

17068076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13449078-G-A

17068116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13449118-T-A

17068156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13449158-T-G

17068160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13449162-T-C

17068170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13449172-G-A

17068170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13449172-G-T

17068386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449458-T-C

17068424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449494-T-C

17068438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449508-A-T

17068471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449538-T-A

17068490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449553-A-G

17068490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449553-A-T

17068544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449678-T-C

17068574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449708-G-A

17068574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449708-G-T

17068575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449709-G-A

17068575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449709-G-C

17068575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449709-G-T

17068595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449722-A-G

17068650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13449777-T-C

17068729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13449856-C-T

17068780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449911-G-A

17068780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449911-G-C

http://identifiers.org/hco/10/GRCh38#17068809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13449941-C-A

17068809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13449941-C-T

17070804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13450025-T-C

17070838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13450059-C-T

17070980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13450194-T-C

17071279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13450548-T-C

17071306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13450575-T-C

17071369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13450711-A-G

17071567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13450920-G-A

17071567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13450920-G-C

17071613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13450966-A-G

17071619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13450972-A-G

17071619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13450972-A-T

http://identifiers.org/hco/10/GRCh38#17071624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13450977-A-C

17071630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13450983-G-T

17071959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13451889-C-T

http://identifiers.org/hco/10/GRCh38#17072054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13451984-A-C

17072054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13451984-A-G

17072055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13451985-T-C

17072063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13451993-T-A

17072098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13452025-T-C

17072175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13452106-A-G

http://identifiers.org/hco/10/GRCh38#17072371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13452286-A-C

17072377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13452292-G-A

17072459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13452373-G-A

17072459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13452373-G-T

17072605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13452456-A-G

17072621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13452474-C-T

17072789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13452650-T-C

17072909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13452780-A-G

http://identifiers.org/hco/10/GRCh38#17072937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13452810-C-A

17073080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13452936-T-C

17073172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13453003-T-A

17073172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13453003-T-C

http://identifiers.org/hco/10/GRCh38#17073218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13453048-C-A

17073918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13453542-G-A

http://identifiers.org/hco/10/GRCh38#17074024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13453644-C-A

17074024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13453644-C-T

17074155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13453773-C-T

http://identifiers.org/hco/10/GRCh38#17074187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13453804-C-A

17074243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13453810-G-A

http://identifiers.org/hco/10/GRCh38#17074669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13454287-C-A

17074702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13454320-G-A

17074711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13454326-A-G

17074748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13454364-G-A

17074748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13454364-G-T

17074787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13454403-C-T

17074818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13454424-T-C

http://identifiers.org/hco/10/GRCh38#17075451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13454693-C-A

17075474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13454716-T-C

17075741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13454917-C-G

17075771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13454945-A-G

17075894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13455158-A-G

17075946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13455211-T-C

17075971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13455237-C-T

17076100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13455365-A-G

17076199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13455461-T-G

http://identifiers.org/hco/10/GRCh38#17076478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13455719-C-A

17076478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13455719-C-T

17076518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13455749-T-A

17076548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13455779-C-T

17076590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13455820-A-G

17076605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13455833-T-C

17076828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13456049-T-C

http://identifiers.org/hco/10/GRCh38#17076851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13456069-C-A

17076951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13456168-C-T

17077058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13456276-T-A

17077058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13456276-T-C

17077252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13456834-T-C

17077439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13457005-G-A

17077439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13457005-G-C

17077586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13457155-C-G

17077586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13457155-C-T

17077594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13457163-C-T

17077624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13457193-G-A

17078209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13457643-G-A

17078229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13457662-G-A

17078229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13457662-G-T

17078301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13457727-A-G

17078364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13457823-T-C

17078375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13457834-T-A

http://identifiers.org/hco/10/GRCh38#17080542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13458661-C-A

17080542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13458661-C-T

17080716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13458808-C-T

17080719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13458811-C-T

17080726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13458818-C-T

17082086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13459333-C-G

17082086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13459333-C-T

17082139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13459384-G-C

http://identifiers.org/hco/10/GRCh38#17082195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13459444-C-A

17082271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13459514-G-A

17084207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13460097-C-T

http://identifiers.org/hco/10/GRCh38#17084385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13460274-A-C

17084408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13460297-G-A

17084421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13460310-A-G

17084501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13460392-A-T

17084518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13460409-G-A

17084518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13460409-G-T

17084520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13460411-A-G

17084612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13460491-T-C

17084822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13460701-A-G

17084874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13460744-T-G

http://identifiers.org/hco/10/GRCh38#17085155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13460999-A-C

17085188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461025-T-C

17085226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461057-T-G

17085254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461084-T-C

http://identifiers.org/hco/10/GRCh38#17085323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13461161-C-A

17085413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461249-A-G

http://identifiers.org/hco/10/GRCh38#17085498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13461323-A-C

17085498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461323-A-T

17085520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461339-A-G

17085546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461365-T-A

17085546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461365-T-C

17085546-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461365-T-G

17085549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461368-C-T

17085583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461402-G-A

17085583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461402-G-C

17085588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461407-G-T

17085643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13461462-G-A

17085673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13461492-G-A

17085806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461632-A-T

17085811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461637-A-G

17085852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13461678-T-A

http://identifiers.org/hco/10/GRCh38#17085905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13461782-C-A

17086635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13462604-T-G

17087182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463148-A-G

17087196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463162-G-T

17087225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463191-G-A

17087227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463193-A-G

http://identifiers.org/hco/10/GRCh38#17087301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13463265-C-A

17087301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463265-C-T

17087394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463348-C-G

17087394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463348-C-T

17087429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463383-G-A

17087683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463426-C-G

17087683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463426-C-T

17088093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463651-G-A

17088093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463651-G-T

17088094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463652-C-G

17088107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463664-T-C

http://identifiers.org/hco/10/GRCh38#17088120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13463677-C-A

17088120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463677-C-T

17088132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463689-G-A

17088132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463689-G-T

17088136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463693-T-A

17088136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463693-T-C

17088147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463704-T-A

17088409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13463996-A-G

17088457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13464044-G-A

17088457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13464044-G-C

17088457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13464044-G-T

17088576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13464155-G-A

17088589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13464167-C-T

17088611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13464192-G-A

17088624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13464205-G-A

17088694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13464305-A-G

17088722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13464333-T-A

17089070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13465061-T-C

17089101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13465086-C-T

17089116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13465100-C-T

17089159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13465141-T-C

17089276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13465250-T-C

17089276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13465250-T-G

17089383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13465363-G-A

17089442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13465415-A-G

17089610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13465558-G-A

17089671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13465617-A-G

17089705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13465651-T-C

17089804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13465723-G-A

http://identifiers.org/hco/10/GRCh38#17090355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13465954-C-A

17090392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13465990-G-A

17090430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13466025-A-G

17090716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13466434-G-A

17090798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13466517-G-A

17090822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13466541-A-G

http://identifiers.org/hco/10/GRCh38#17090863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13466562-A-C

17090909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13466588-C-T

17091021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13466679-T-C

17091066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13466721-G-A

17091075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13466731-C-G

17091075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13466731-C-T

17091241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13466860-C-T

http://identifiers.org/hco/10/GRCh38#17091409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13466989-A-C

http://identifiers.org/hco/10/GRCh38#17092967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13467979-A-C

17093019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13468018-T-C

17093031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13468032-C-T

17093049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13468050-T-C

17093049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13468050-T-G

17093082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13468105-A-G

17093130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13468156-G-A

17093320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13468347-T-C

17093661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13468639-G-A

17099954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13470581-A-G

17100030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13470651-T-C

http://identifiers.org/hco/10/GRCh38#17100042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13470663-C-A

17100042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13470663-C-T

17100045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13470666-A-G

17100046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13470667-T-C

17100102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13470723-T-C

17100108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13470729-A-T

17100201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13470822-G-C

17100230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13470851-T-C

17100276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13470882-T-C

17100276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13470882-T-G

17101250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13471162-A-G

17101360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13471268-G-A

17101423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13471331-T-C

17101498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13471416-A-T

17101681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13471619-G-A

17101800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13471727-A-T

17101836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13471763-T-C

17101946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13471845-G-A

http://identifiers.org/hco/10/GRCh38#17102026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13471922-C-A

17102026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13471922-C-T

17102945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13472233-T-C

17103209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13472505-A-G

17103220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: 13472516-A-G

17103259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13472558-G-T

17103266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13472565-T-C

17103523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13472760-C-T

http://identifiers.org/hco/10/GRCh38#17103737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13472957-A-C

17103737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13472957-A-G

17103740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13472960-G-T

http://identifiers.org/hco/10/GRCh38#17103795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13473019-A-C

17103905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13473043-G-A

17103944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13473082-T-A

17103944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13473082-T-C

17104169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13473283-A-G

17104304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13473414-T-A

17104304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13473414-T-C

17104305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13473415-A-G

17104355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13473462-G-T

17104612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 13473718-G-A

http://identifiers.org/hco/10/GRCh38#17104624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13473729-C-A

17104624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13473729-C-G

http://identifiers.org/hco/10/GRCh38#17104625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13473730-A-C

17104625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13473730-A-G

17104694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13473798-G-A

17104694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13473798-G-T

17104746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13473863-T-C

17105597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13474716-C-T

17105621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13474737-T-C

17105664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13474779-A-T

17105699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13474814-G-A

17105699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13474814-G-T

17105721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13474836-G-A

17105746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13474861-T-C

17105827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13474925-A-T

http://identifiers.org/hco/10/GRCh38#17105875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13474971-C-A

17105875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13474971-C-G

17107012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13475536-A-T

17107205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13475698-A-G

17107405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13475896-A-G

http://identifiers.org/hco/10/GRCh38#17108759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13477235-C-A

17108969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13477443-T-C

17109012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13477487-G-C

17109064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13477536-T-A

17109076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13477547-T-A

17109203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13477662-G-A

17109203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13477662-G-C

17109203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13477662-G-T

17109207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13477666-T-C

17109506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13477956-T-C

17109507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13477957-G-T

17109512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13477962-G-A

17109512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13477962-G-C

17109512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13477962-G-T

17109516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13477966-T-A

17109524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13477972-G-T

17109530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13477978-A-T

17109577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13478143-G-T

http://identifiers.org/hco/10/GRCh38#17109611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13478181-C-A

17109611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13478181-C-T

17109662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, undefined
orthologous variants: 13478237-A-T

17109801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13478377-A-G

17109801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13478377-A-T

17110150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13479430-G-A

17110224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13479505-G-A

http://identifiers.org/hco/10/GRCh38#17110275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13479531-A-C

17110289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13479545-C-G

17110345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13479605-C-T

17110400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13479632-T-C

17110466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13479694-C-G

17110865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13480806-T-C

17110995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: synonymous variant
orthologous variants: 13480924-G-A

17111066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13480993-G-A

17111066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13480993-G-T

17111079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13481006-A-T

17111112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13481037-A-G

17111112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13481037-A-T

17111180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13481307-A-G

17111196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13481324-T-C

17111295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13481419-A-G

17111454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13481543-G-A

17111489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13481561-T-C

17111527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13481597-T-G

17111660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13481687-A-T

http://identifiers.org/hco/10/GRCh38#17111663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13481690-C-A

17111663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13481690-C-T

17112130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13481884-T-C

17112148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13481900-T-A

17112153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13481905-A-G

17112253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13482002-G-T

17112266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13482016-T-C

17112357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13482100-T-G

17112539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13482295-T-A

17112539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13482295-T-C

17112606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13482363-C-T

17112673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13482414-T-C

17112715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13482449-C-T

17113839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13482701-G-T

17113857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13482719-T-C

http://identifiers.org/hco/10/GRCh38#17113909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13482763-A-C

17113909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13482763-A-G

17114188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 13483032-G-A

http://identifiers.org/hco/10/GRCh38#17114272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13483114-C-A

17114274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13483116-G-A

17114274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13483116-G-T

http://identifiers.org/hco/10/GRCh38#17114287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13483133-C-A

17114287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13483133-C-G

17114287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13483133-C-T

http://identifiers.org/hco/10/GRCh38#17114327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13483173-C-A

17114396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13483240-C-T

http://identifiers.org/hco/10/GRCh38#17114422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13483266-C-A

17114531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13483364-G-A

17114857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13483637-T-C

http://identifiers.org/hco/10/GRCh38#17115321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13483727-C-A

17115321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13483727-C-T

17115422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13483835-T-C

http://identifiers.org/hco/10/GRCh38#17115501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13483911-A-C

http://identifiers.org/hco/10/GRCh38#17115527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13483937-C-A

17115616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13484026-C-G

17115718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13484120-G-A

17115718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13484120-G-T

17115734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13484136-T-G

17115787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13484189-T-A

17115788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13484190-G-A

17116254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13484580-T-A

17116321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13484646-T-A

17116380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13484698-G-A

http://identifiers.org/hco/10/GRCh38#17116398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13484715-C-A

17116559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13484844-C-T

http://identifiers.org/hco/10/GRCh38#17116613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13484940-A-C

17116614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13484941-A-G

http://identifiers.org/hco/10/GRCh38#17116639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13484965-A-C

17116639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13484965-A-T

17116683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13485006-T-C

17117031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13485321-T-C

17117734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13485596-A-G

17117778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13485647-G-T

17117835-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13485704-C-G

17117835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13485704-C-T

17117847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13485716-C-G

17117877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13485747-C-T

17118164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13485977-C-T

17118924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13486944-T-C

17119133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13487217-C-T

17119299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13487373-C-T

17119328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13487397-T-C

17119334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13487403-G-A

17119685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13487437-G-A

17119714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13487465-C-G

17119816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13487560-A-G

http://identifiers.org/hco/10/GRCh38#17119868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13487630-A-C

17119869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13487631-C-T

17119870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13487632-C-G

17120161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13487899-T-G

17120215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13487954-A-G

17120372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13488887-G-A

17120435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13488952-T-C

17120685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13489165-T-A

17120966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13489453-C-T

http://identifiers.org/hco/10/GRCh38#17121063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13489589-A-C

17121839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13489950-G-T

17121841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13489952-T-A

17121841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13489952-T-C

http://identifiers.org/hco/10/GRCh38#17121860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13489971-C-A

17121860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13489971-C-G

http://identifiers.org/hco/10/GRCh38#17122002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13490112-C-A

17122016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490126-G-A

17122030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490141-T-C

17122171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490246-G-T

http://identifiers.org/hco/10/GRCh38#17122214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13490293-A-C

17122214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490293-A-G

17122233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490313-T-C

17122233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490313-T-G

17122260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490338-T-C

17122273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490362-G-A

17122284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490383-G-A

http://identifiers.org/hco/10/GRCh38#17122302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13490401-C-A

17122302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490401-C-G

17122302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490401-C-T

17122412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490507-G-A

17122412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490507-G-T

17122426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490521-T-G

17122504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490598-T-C

17122515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490608-G-A

17122515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490608-G-C

17122515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 13490608-G-T

17122559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, missense_variant
orthologous variants: 13490649-T-A

http://identifiers.org/hco/10/GRCh38#17122589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13490679-C-A

17122646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13490722-G-A

17122765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13490838-A-T

17122926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13490989-G-A

17122943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13491006-G-T

17122992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13491054-A-G

17123044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron variant
orthologous variants: 13491103-T-C

17123374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, undefined
orthologous variants: 13491384-T-C

17123501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 13491469-G-T

17123714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13491698-T-A

17123714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13491698-T-C

17123765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13491755-G-A

17123765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13491755-G-T

http://identifiers.org/hco/10/GRCh38#17123785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13491767-C-A

17123940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13491985-G-A

17123966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13492017-G-A

17124341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13492458-C-T

17124344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13492461-G-C

http://identifiers.org/hco/10/GRCh38#17125261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13492612-C-A

17125314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13492643-C-T

17125323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13492652-A-G

17125334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13492665-A-G

17125784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13493101-G-A

17125920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13493275-C-T

17126197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13493433-A-G

17126347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13493574-T-C

17126390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13493612-C-T

17126510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13493737-G-A

http://identifiers.org/hco/10/GRCh38#17126612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13493827-C-A

17126612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13493827-C-T

http://identifiers.org/hco/10/GRCh38#17126614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13493829-C-A

17126614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13493829-C-G

17126614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13493829-C-T

http://identifiers.org/hco/10/GRCh38#17126618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13493833-C-A

17126618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13493833-C-T

17126672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13493904-T-C

17126676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13493908-C-T

17126688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494059-G-T

17126751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494120-T-A

17126751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494120-T-G

17126805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 13494176-A-T

17126807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 13494178-T-A

17126807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 13494178-T-C

17126843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494214-C-T

http://identifiers.org/hco/10/GRCh38#17126927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13494287-C-A

http://identifiers.org/hco/10/GRCh38#17126946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13494306-C-A

17126946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494306-C-T

http://identifiers.org/hco/10/GRCh38#17126948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13494308-C-A

17126988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494333-C-T

17127134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494464-G-C

17127142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494472-G-A

17127629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494520-T-A

17127797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494669-A-G

17127797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494669-A-T

17127844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13494724-A-G

17127887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13494767-C-T

17127946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494826-G-T

17127949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494829-A-G

17127964-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494844-G-C

17127964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494844-G-T

http://identifiers.org/hco/10/GRCh38#17128036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13494882-C-A

17128036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494882-C-T

17128120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13494927-T-C

17128460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13495298-T-C

http://identifiers.org/hco/10/GRCh38#17128466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13495304-C-A

http://identifiers.org/hco/10/GRCh38#17128548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13495383-C-A

17128630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13495510-A-G

http://identifiers.org/hco/10/GRCh38#17129041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#13495911-A-C

17129096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13495967-C-T

17129438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13496310-T-C

17129439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13496311-T-G

17129540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13496415-A-G

17129631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 13496499-T-C

17129661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13496529-T-C

17129673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13496541-C-T

17129686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13496554-T-A

17129686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13496554-T-C

17129700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 13496568-A-G

17129761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2548
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 13496629-A-G