http://identifiers.org/hco/5/GRCh38#80052452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92916792-C-A

http://identifiers.org/hco/5/GRCh38#80052496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92916766-A-C

80052501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92916761-T-C

80052509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92916748-A-G

80052509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92916748-A-T

80052548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92916708-A-G

80052605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92916674-T-C

80052618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92916661-A-G

http://identifiers.org/hco/5/GRCh38#80052927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92916385-C-A

80052975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92916287-G-A

http://identifiers.org/hco/5/GRCh38#80053082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92916048-C-A

80053159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92915948-T-A

80053159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92915948-T-C

80055406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92913946-T-C

80055589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92913765-G-A

http://identifiers.org/hco/5/GRCh38#80055657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92913697-C-A

80055657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92913697-C-T

http://identifiers.org/hco/5/GRCh38#80055787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#92913616-A-C

80055787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 92913616-A-G

80055788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92913615-T-C

80055808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92913595-G-A

80055808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92913595-G-T

80055811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92913592-G-C

80055931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92913472-T-G

80055939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92913464-G-A

80055946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92913457-T-C

http://identifiers.org/hco/5/GRCh38#80056093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92913313-C-A

80056093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92913313-C-T

80056099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92913307-A-T

80056178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92913236-G-A

80056178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92913236-G-C

80056178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92913236-G-T

80056394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92913017-G-A

80056394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92913017-G-T

80056398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92913013-T-C

http://identifiers.org/hco/5/GRCh38#80058337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92912583-C-A

80058337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92912583-C-G

80058337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92912583-C-T

80058343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92912577-T-A

80058343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92912577-T-C

80058343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92912577-T-G

80058397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92912530-G-A

80058397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92912530-G-T

80058408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92912520-A-G

80058588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92912344-A-G

80058592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92912340-T-C

80058592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92912340-T-G

80058686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92912093-T-C

80058879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911912-C-G

80058879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911912-C-T

http://identifiers.org/hco/5/GRCh38#80058891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92911897-C-A

80058891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911897-C-G

http://identifiers.org/hco/5/GRCh38#80058913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92911874-C-A

80058913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911874-C-T

http://identifiers.org/hco/5/GRCh38#80058914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92911873-A-C

80058914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911873-A-G

80058960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911834-G-T

80059355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911751-T-A

80059355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911751-T-C

80059357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911749-G-A

80059357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911749-G-C

80059357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911749-G-T

80059361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911745-G-C

80059361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911745-G-T

80059368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911738-A-G

80059371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911735-G-C

80059371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911735-G-T

80059386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911721-G-C

80059386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911721-G-T

80059392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911715-T-C

80059392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911715-T-G

http://identifiers.org/hco/5/GRCh38#80059411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92911696-A-C

80059411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911696-A-G

80059426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911680-T-A

80059522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911591-G-A

80059522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911591-G-T

80059582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911512-G-C

80059640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911456-T-G

80059647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911449-C-T

80059666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911430-G-A

80059932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911159-G-T

http://identifiers.org/hco/5/GRCh38#80059936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92911155-C-A

80059995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92911102-G-A

80060200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910895-A-G

80060449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910682-A-G

80060812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910629-C-G

80060817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910624-C-G

80060870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910587-C-T

80060904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910558-G-C

80060962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910521-A-G

80061063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910411-C-G

80061139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910334-T-C

80061157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910303-T-G

80061211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910246-G-A

80061211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910246-G-C

80061212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910245-A-G

80061379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910097-T-C

80061402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910087-G-T

80061427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910062-A-G

80061427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92910062-A-T

80061617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92909877-G-T

http://identifiers.org/hco/5/GRCh38#80061634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92909860-A-C

80061797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92909698-G-A

80061833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 92909662-G-A

80061905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92909600-G-T

80061941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92909565-G-T

80061956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92909550-G-A

80062080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92909415-A-G

http://identifiers.org/hco/5/GRCh38#80062105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92909389-C-A

80063649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92908927-G-T

80063835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92908674-C-T

80063984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92908578-G-A

80064131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92908430-C-T

80064364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92908246-G-A

http://identifiers.org/hco/5/GRCh38#80065280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92906228-C-A

80065280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92906228-C-T

http://identifiers.org/hco/5/GRCh38#80065296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92906209-C-A

80065296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92906209-C-T

http://identifiers.org/hco/5/GRCh38#80065530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92905998-A-C

http://identifiers.org/hco/5/GRCh38#80065620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92905911-C-A

80065620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92905911-C-T

80066670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92905519-A-G

80066742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92905447-C-T

80066808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92905389-A-G

80066968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92905237-T-A

80067247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92904844-A-G

80067508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92904226-G-A

80067508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92904226-G-T

http://identifiers.org/hco/5/GRCh38#80067517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92904217-C-A

http://identifiers.org/hco/5/GRCh38#80067619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92904136-C-A

80067619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92904136-C-G

80067626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92904129-G-T

80067659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92904097-T-C

80067724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92904031-C-G

80067724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92904031-C-T

http://identifiers.org/hco/5/GRCh38#80067757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92903996-C-A

80067757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92903996-C-T

80067783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92903970-T-C

http://identifiers.org/hco/5/GRCh38#80067824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92903924-C-A

http://identifiers.org/hco/5/GRCh38#80067825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92903923-A-C

80067825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92903923-A-T

80067856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92903892-G-A

80067856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92903892-G-T

80068142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92903647-C-T

80068234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92903539-T-A

80068261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92903502-A-G

http://identifiers.org/hco/5/GRCh38#80068672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92903273-C-A

80068672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92903273-C-T

80068822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92903159-T-C

80068862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92903133-G-A

80068902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92903094-T-C

80069224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92902768-T-A

80069587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92902365-C-G

http://identifiers.org/hco/5/GRCh38#80069660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92902292-A-C

80069836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92902129-G-A

80070020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92901981-G-C

80070153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900287-G-A

80070241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900203-T-A

80070241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900203-T-C

80070422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900027-G-A

80070422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900027-G-C

80070422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900027-G-T

http://identifiers.org/hco/5/GRCh38#80070430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92900019-A-C

80070430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900019-A-G

80070431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900018-G-A

80070442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900007-T-A

80070442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92900007-T-C

80070462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92899987-T-A

80070462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92899987-T-C

http://identifiers.org/hco/5/GRCh38#80070579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92899859-C-A

80070586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92899852-A-G

http://identifiers.org/hco/5/GRCh38#80070628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92899804-C-A

80070697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92899735-A-G

80070703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92899729-G-A

80070706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92899726-G-A

80070712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92899720-G-A

80070712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92899720-G-T

80070718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92899714-G-C

80070774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92899658-T-C

http://identifiers.org/hco/5/GRCh38#80070790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92899642-C-A

80070790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92899642-C-G

80070917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92899503-A-G

80071240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92899214-T-C

80071240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92899214-T-G

80071301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92899176-G-A

80071302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92899175-G-A

80071687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92898672-T-A

80071687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92898672-T-C

80071687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92898672-T-G

http://identifiers.org/hco/5/GRCh38#80071688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92898671-A-C

80071688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92898671-A-G

80071688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92898671-A-T

http://identifiers.org/hco/5/GRCh38#80071713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92898645-C-A

80071713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92898645-C-T

http://identifiers.org/hco/5/GRCh38#80071715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92898643-C-A

http://identifiers.org/hco/5/GRCh38#80071756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92898602-C-A

80071771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92898560-A-G

80071795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92898534-G-A

80071795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92898534-G-T

80071828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92898501-T-C

http://identifiers.org/hco/5/GRCh38#80071992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92898371-C-A

http://identifiers.org/hco/5/GRCh38#80072072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92898290-C-A

80072072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92898290-C-G

http://identifiers.org/hco/5/GRCh38#80072241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92898126-C-A

80072241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92898126-C-T

http://identifiers.org/hco/5/GRCh38#80072438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92897933-C-A

80072562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92897794-G-A

80072562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92897794-G-T

80072575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92897772-G-C

80072575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92897772-G-T

80072577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92897762-T-C

80072577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92897762-T-G

80072588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92897751-A-G

http://identifiers.org/hco/5/GRCh38#80072593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92897745-C-A

80072593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92897745-C-T

80072594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92897744-T-C

80072598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92897740-T-C

80072624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92897715-T-C

80072643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92897696-G-A

80072643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92897696-G-C

80072643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92897696-G-T

http://identifiers.org/hco/5/GRCh38#80072760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92897599-C-A

80072760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897599-C-G

80072760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897599-C-T

80072777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897582-G-T

80072802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897559-C-T

80072828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897535-G-A

http://identifiers.org/hco/5/GRCh38#80072872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92897489-A-C

80072966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897397-T-C

http://identifiers.org/hco/5/GRCh38#80073079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92897286-A-C

80073254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897111-C-T

80073408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897001-G-A

80073408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897001-G-C

80073408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92897001-G-T

80073757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92896927-G-T

80073827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92896863-T-G

80074045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92896692-A-G

80074047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92896691-A-G

80074212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92896565-G-T

80074257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 92896529-T-C

80074281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92896506-A-G

http://identifiers.org/hco/5/GRCh38#80074322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92896468-C-A

80074490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92896204-A-G

80075261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92896061-G-T

80075365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92895962-A-G

80075434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895909-T-C

80075436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895907-G-T

80075451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895894-G-A

80075451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895894-G-T

http://identifiers.org/hco/5/GRCh38#80075475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92895870-C-A

80075609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895738-C-T

80075676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895671-T-C

80075692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895655-G-C

80075974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92895425-G-T

80076113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92895280-G-T

80076122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92895271-A-G

80076132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92895261-A-G

http://identifiers.org/hco/5/GRCh38#80076181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92895209-C-A

80076233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92895183-A-G

80076251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92895165-G-A

80076251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92895165-G-C

80076304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92895109-T-C

http://identifiers.org/hco/5/GRCh38#80076354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92895069-C-A

http://identifiers.org/hco/5/GRCh38#80076381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92895042-C-A

80076381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92895042-C-T

http://identifiers.org/hco/5/GRCh38#80076759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92894695-A-C

80076759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92894695-A-G

80076759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92894695-A-T

http://identifiers.org/hco/5/GRCh38#80076774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92894683-C-A

80076774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92894683-C-T

http://identifiers.org/hco/5/GRCh38#80076779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92894678-A-C

80076779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92894678-A-G

80076779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92894678-A-T

http://identifiers.org/hco/5/GRCh38#80076784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92894673-C-A

http://identifiers.org/hco/5/GRCh38#80076795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92894664-A-C

80076795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92894664-A-G

80076961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92894515-G-C

80076961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92894515-G-T

80076967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92894509-A-G

80076982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92894494-G-A

http://identifiers.org/hco/5/GRCh38#80077058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92894418-C-A

80077068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92894408-A-G

http://identifiers.org/hco/5/GRCh38#80077070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92894406-C-A

80077070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92894406-C-G

80077109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92894359-G-A

80077109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92894359-G-T

80077790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92893914-T-G

80077792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92893912-G-A

80077978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92893148-C-T

80078005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92893127-G-T

http://identifiers.org/hco/5/GRCh38#80078012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92893120-C-A

80078012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92893120-C-G

80078012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92893120-C-T

http://identifiers.org/hco/5/GRCh38#80078030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92893108-C-A

80078030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92893108-C-T

80078084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92893057-G-A

80078084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92893057-G-T

http://identifiers.org/hco/5/GRCh38#80078099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#92893042-A-C

80078099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92893042-A-G

80078104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92893037-T-C

80078120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92893021-C-T

80078192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92892949-G-A

80078226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 92892853-A-G

80078231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92892848-A-G

http://identifiers.org/hco/5/GRCh38#80078255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92892787-C-A

80078255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92892787-C-T

http://identifiers.org/hco/5/GRCh38#80078263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92892779-C-A

80078263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92892779-C-T

http://identifiers.org/hco/5/GRCh38#80078264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92892778-C-A

80078370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92892615-G-A

80078384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92892602-T-C

80078408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92892584-T-C

80078672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92892102-C-T

80078697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92892077-G-A

http://identifiers.org/hco/5/GRCh38#80078745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92892065-C-A

80078745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92892065-C-T

80078748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92892062-A-G

80078748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92892062-A-T

80078761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92892049-G-A

80078761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92892049-G-T

80078768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92892042-A-G

80078768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92892042-A-T

80078971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 92891873-T-A

http://identifiers.org/hco/5/GRCh38#80079007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92891839-C-A

80079007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92891839-C-T

http://identifiers.org/hco/5/GRCh38#80079220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#92891633-C-A

80079343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92891510-T-C

80079360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92891495-A-G

80079383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92891472-A-T

80079450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92891401-A-G

80079456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92891395-G-A

80079515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92891335-A-G

http://identifiers.org/hco/5/GRCh38#80079539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92891307-A-C

80079615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92891236-A-G

80079640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92891211-G-A

80079693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92891159-T-C

80079814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92891036-G-A

80079862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890989-T-C

80079968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92890883-A-G

80080001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92890850-T-C

80080984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890425-T-C

80081304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92890121-A-G

80081722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92889756-T-G

80081728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92889748-T-C

80081729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92889747-G-A

80081735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92889712-G-T

80081844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889453-G-A

80082080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889245-G-A

80082100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889215-T-C

80082100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889215-T-G

http://identifiers.org/hco/5/GRCh38#80082108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92889207-A-C

80082108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889207-A-G

80082121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889197-G-A

80082121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889197-G-T

80082149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889169-G-A

80082149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889169-G-T

80082164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889156-G-A

80082164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889156-G-T

http://identifiers.org/hco/5/GRCh38#80082195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92889154-C-A

80082195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889154-C-T

80082269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889093-G-A

80082269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889093-G-T

http://identifiers.org/hco/5/GRCh38#80082272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92889090-A-C

80082272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889090-A-G

80082295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889076-G-A

80082295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92889076-G-T

80082333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92889035-C-T

http://identifiers.org/hco/5/GRCh38#80082344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92889025-A-C

80082345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92889024-C-G

80082422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 92888983-G-T

80082588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92888819-T-G

http://identifiers.org/hco/5/GRCh38#80082629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92888783-C-A

80082629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92888783-C-G

http://identifiers.org/hco/5/GRCh38#80082634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92888778-A-C

http://identifiers.org/hco/5/GRCh38#80082668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92888738-C-A

80082668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92888738-C-T

80082684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92888716-A-G

80082849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92888551-T-A

80082849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92888551-T-G

80082897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92888503-A-G

http://identifiers.org/hco/5/GRCh38#80082971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#92888429-C-A

http://identifiers.org/hco/5/GRCh38#80083381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92887995-C-A

80083470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92887891-A-T

80083520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: non coding transcript exon variant
orthologous variants: 92887850-G-A

80083520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: non coding transcript exon variant
orthologous variants: 92887850-G-T

http://identifiers.org/hco/5/GRCh38#80083572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92887795-C-A

80083572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: non coding transcript exon variant
orthologous variants: 92887795-C-T

80083597-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: non coding transcript exon variant
orthologous variants: 92887772-A-T

http://identifiers.org/hco/5/GRCh38#80083635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#92887751-C-A

80083635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: non coding transcript exon variant
orthologous variants: 92887751-C-T

80083640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40583
most severe consequence: non coding transcript exon variant
orthologous variants: 92887746-C-T