24429255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75157876-G-T

24429266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75157885-G-A

24429266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75157885-G-T

24429275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75157894-A-G

24429280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75157899-T-A

24429284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75157903-G-T

24429310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75157928-G-A

http://identifiers.org/hco/22/GRCh38#24429355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75157973-C-A

24429433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75158048-A-G

24429493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75158104-G-T

24429567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75158184-T-C

24429678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75158481-C-G

24429678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75158481-C-T

24429680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75158483-G-A

24429681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75158484-A-G

http://identifiers.org/hco/22/GRCh38#24429766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75158565-C-A

24429766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75158565-C-G

http://identifiers.org/hco/22/GRCh38#24429921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75158711-C-A

24429921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75158711-C-T

24430046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75158830-T-A

24430046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75158830-T-G

24430126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75158906-T-C

24430228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75159008-G-A

24430228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75159008-G-T

24430315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75159066-G-A

24430348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75159098-G-A

24430348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75159098-G-T

24430359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75159108-A-G

24430359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75159108-A-T

24430390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159135-G-A

24430390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159135-G-T

24430392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159137-A-G

24430406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159148-T-A

24430406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159148-T-C

24430409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159151-A-G

24430427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159169-A-G

24430433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159175-A-G

24430444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159186-T-G

http://identifiers.org/hco/22/GRCh38#24430449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75159191-C-A

24430449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159191-C-T

24430502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159240-G-T

24430734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159474-C-T

24430751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159491-T-A

24430751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159491-T-C

http://identifiers.org/hco/22/GRCh38#24430802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75159541-C-A

24430802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159541-C-G

24430802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159541-C-T

http://identifiers.org/hco/22/GRCh38#24430815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75159555-C-A

24430822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159562-G-A

24430823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159563-G-T

24430832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75159584-G-T

24430899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75159672-G-A

24430899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75159672-G-T

24431110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75159801-G-A

24431110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75159801-G-T

24431264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75159973-C-G

http://identifiers.org/hco/22/GRCh38#24431411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#75160060-C-A

24431411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75160060-C-T

24431438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75160083-G-C

24431438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75160083-G-T

24431443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75160088-G-A

24431443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75160088-G-C

24431601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75160217-A-G

24431670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75160267-C-T

24431679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75160276-G-A

24431679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75160276-G-T

24431689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75160286-G-C

24431689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75160286-G-T

24431716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75160335-G-T

http://identifiers.org/hco/22/GRCh38#24431752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75160374-A-C

24431756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75160379-G-T

24431758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75160381-A-G

24432138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75160738-G-A

24432138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75160738-G-T

24432178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75160771-G-A

24432204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75160798-G-A

24432204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75160798-G-T

24432286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75160911-C-G

24432286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75160911-C-T

24432338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75160963-G-A

24432338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75160963-G-T

24432360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75160981-G-A

24432374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75160994-T-C

http://identifiers.org/hco/22/GRCh38#24432376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75160996-C-A

24432376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75160996-C-T

24432382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75161002-G-A

24432382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75161002-G-C

24432382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75161002-G-T

24432406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75161018-G-T

24432421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75161034-G-A

24432421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75161034-G-T

24432442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75161055-G-T

24432455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161075-G-A

24432455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161075-G-T

24432472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161092-G-T

http://identifiers.org/hco/22/GRCh38#24432484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75161104-C-A

24432484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161104-C-T

24432493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161113-A-G

24432493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161113-A-T

24432523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161145-G-T

24432525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161147-A-G

24432545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161167-T-C

http://identifiers.org/hco/22/GRCh38#24432581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75161202-C-A

24432581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161202-C-G

24432581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161202-C-T

24432651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161283-C-T

http://identifiers.org/hco/22/GRCh38#24432692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#75161324-A-C

24432702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161331-G-A

24432702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161331-G-T

http://identifiers.org/hco/22/GRCh38#24432732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75161363-C-A

24432763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161396-G-A

24432786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161418-A-G

http://identifiers.org/hco/22/GRCh38#24432846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#75161475-C-A

24432846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161475-C-G

http://identifiers.org/hco/22/GRCh38#24432948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75161513-C-A

24432948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161513-C-G

24432948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161513-C-T

24433005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161552-T-C

24433005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75161552-T-G

http://identifiers.org/hco/22/GRCh38#24433138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#75161626-A-C

24433138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161626-A-G

24433146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161633-T-C

24433164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161651-T-C

24433164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161651-T-G

24433202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161681-C-T

24433329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161780-G-A

24433329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161780-G-T

24433332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161783-G-A

24433332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161783-G-T

24433333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161784-G-A

24433333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75161784-G-T

24433575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75162024-G-C

24433617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75162066-C-T

24433620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75162069-T-A

24433668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75162117-G-A

24434192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75162502-C-T

http://identifiers.org/hco/22/GRCh38#24434675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75162927-C-A

24434782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75163032-T-G

24434806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75163049-A-G

24434990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75163230-C-G

24434990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75163230-C-T

24435259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75163617-G-A

24435295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75163653-G-A

24435459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75163810-G-A

24435601-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75163944-G-C

24436360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75164602-A-G

24436620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75164857-T-A

24436861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75165283-C-T

24436992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75165421-G-T

24437145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75165574-A-T

24437266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75165689-C-T

24437297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75165718-G-C

24437297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75165718-G-T

24437914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75166345-T-C

24437934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75166365-C-G

24438136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75166500-T-C

http://identifiers.org/hco/22/GRCh38#24438182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75166545-C-A

24438541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75166877-G-T

24438698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75167117-T-C

24438977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75167342-T-C

24439073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75167386-T-A

24439073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75167386-T-C

24439073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75167386-T-G

http://identifiers.org/hco/22/GRCh38#24439175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75167472-C-A

http://identifiers.org/hco/22/GRCh38#24439184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75167481-A-C

24439184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75167481-A-G

24439184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75167481-A-T

http://identifiers.org/hco/22/GRCh38#24439208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75167512-A-C

24439208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75167512-A-G

24439232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75167535-G-A

24439388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75167855-T-C

24439581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75168028-G-T

24439609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75168056-C-T

24439837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75168259-G-C

24439850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75168272-T-C

24440495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75168779-G-A

24440495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75168779-G-T

24440516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75168801-G-A

24440516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75168801-G-T

24440613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75168891-T-C

24440865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169137-A-G

24440940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169212-T-C

24441096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169368-T-G

24441348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169620-G-A

24441348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169620-G-T

24441353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169625-G-A

24441353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169625-G-C

http://identifiers.org/hco/22/GRCh38#24441432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#75169686-C-A

24441432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169686-C-T

24441533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169787-T-C

24441560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169815-T-A

24441560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169815-T-C

24441576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169837-A-T

24441695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169944-A-G

24441704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169953-G-T

24441723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169972-G-A

24441723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75169972-G-T

24441778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75170021-C-T

24441872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75170109-C-T

24441902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75170135-T-C

24441902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75170135-T-G

24441906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75170139-G-A

24441906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75170139-G-T

http://identifiers.org/hco/22/GRCh38#24441948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#75170187-C-A

24441948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75170187-C-G

24441948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75170187-C-T

24441974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75170212-C-T

24442022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75170260-C-T

http://identifiers.org/hco/22/GRCh38#24442026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#75170264-C-A

24442039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75170277-T-C

24442039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75170277-T-G

http://identifiers.org/hco/22/GRCh38#24442065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#75170305-C-A

24442065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75170305-C-T

http://identifiers.org/hco/22/GRCh38#24442089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#75170330-C-A

24442131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75170367-A-G

24442131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75170367-A-T

24442137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 75170373-A-G

24442206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75170442-A-G

24442217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75170453-G-A

24442217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75170453-G-T

http://identifiers.org/hco/22/GRCh38#24442223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#75170459-C-A

24442223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75170459-C-G

24442250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 75170486-G-T

24442360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75170633-A-G

24442378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75170651-T-C

24442394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75170668-G-A

http://identifiers.org/hco/22/GRCh38#24442461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75170744-C-A

24442586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75170973-C-T

24442635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75171026-T-A

24442673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75171063-C-T

24442732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75171123-C-T

24442733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75171124-G-A

http://identifiers.org/hco/22/GRCh38#24442861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75171229-C-A

24442861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75171229-C-T

24443034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75171369-G-T

24443190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75171509-A-G

24443757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75171931-T-C

24444032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75172176-G-A

24444106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75172257-C-T

24444154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75172296-G-A

http://identifiers.org/hco/22/GRCh38#24444567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75174418-C-A

24444634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75174471-G-A

http://identifiers.org/hco/22/GRCh38#24444658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75174486-C-A

24444661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75174489-C-G

24444786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75174605-G-A

24444994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75174818-C-T

http://identifiers.org/hco/22/GRCh38#24445015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75174839-C-A

24445015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75174839-C-T

24445101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75174908-C-T

24445150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75174964-C-T

24445677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75175626-C-G

24445911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75175990-G-T

24445953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75176026-G-T

24445992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75176058-G-A

24445992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75176058-G-C

24446571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75176999-T-C

24446603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75177030-G-A

24446818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75177224-C-T

http://identifiers.org/hco/22/GRCh38#24446840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75177246-C-A

24446840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75177246-C-T

24447521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

24447530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

24447531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

24447622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75177727-C-T

24450416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75180117-A-G

24450931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75180672-A-G

24450931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75180672-A-T

http://identifiers.org/hco/22/GRCh38#24450938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75180679-A-C

24451152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75180823-G-A

24451289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75180951-G-A

24451316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75180996-G-A

24451558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75181231-G-A

24451559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75181232-T-C

24451750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75181505-A-G

24454719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75185362-A-G

24455295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75185977-T-C

24455359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75186039-T-C

24455895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75186565-C-T

24456071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75186733-G-A

24456071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75186733-G-T

24456835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75187341-G-C

24456924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75187428-G-C

24456991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75187496-T-C

24460345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75192864-C-T

24460419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75192933-A-G

24460549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75193037-T-C

24460586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75193069-G-T

24460673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75193118-G-A

24460673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75193118-G-T

http://identifiers.org/hco/22/GRCh38#24460739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75193187-C-A

24460777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 75193236-G-T

24460825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75193284-T-C

24460839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75193298-T-C

24462286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196670-A-G

24462338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75196719-C-T

24462837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197052-G-A

24462917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197133-G-A

24463056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197257-A-G

24463056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197257-A-T

24463245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197436-A-G

24466009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197624-C-T

24466058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197668-G-C

http://identifiers.org/hco/22/GRCh38#24466091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75197698-C-A

24466091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197698-C-G

24466091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197698-C-T

24466508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197934-C-T

24466567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75197992-G-A

24466576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75198004-G-A

24466601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75198029-G-A

24467591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200804-G-A

http://identifiers.org/hco/22/GRCh38#24467616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75200815-A-C

24467757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200912-T-C

24467786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200938-C-G

24467843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75200980-T-C

24471463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75209605-G-A

24471470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75209612-G-A

24471546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75209694-T-A

24471661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75209742-A-G

24471677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75209758-G-C

http://identifiers.org/hco/22/GRCh38#24471871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75209931-C-A

24471889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75209949-G-A

24471889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 75209949-G-T

24471971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210032-G-A

24471990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210051-G-A

24471990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210051-G-C

24471990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210051-G-T

24472030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210091-C-G

24472204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75210234-C-T

24473577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75211956-C-T

http://identifiers.org/hco/22/GRCh38#24473642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75212013-C-A

24473906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75212182-A-G

24473957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75212211-C-T

24474352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75212582-G-A

24474653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75212882-C-T

24474717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75212942-G-A

24474765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75212989-T-C

24474882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75213091-A-G

24474895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75213104-A-G

http://identifiers.org/hco/22/GRCh38#24474961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75213173-C-A

24475347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75213483-T-C

24477711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75214336-G-C

24478777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75214794-T-C

24481035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75215607-G-A

24481055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75215627-C-G

24482164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75223735-T-A

24482250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75223803-T-C

24482310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75223866-A-G

24482430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75224686-T-C

24482530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75224785-A-G

24482590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75224847-G-C

24482647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75224901-G-A

24482698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75224949-T-A

24482758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75225157-T-C

24483097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75225399-C-T

24483489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75225633-T-G

24484037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75225872-G-A

http://identifiers.org/hco/22/GRCh38#24484115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75225958-C-A

24484174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75226056-A-G

24484336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75226221-G-C

24484538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75226270-C-T

24484648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75226379-T-G

24485318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75226661-A-G

24485332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75226674-G-A

http://identifiers.org/hco/22/GRCh38#24485613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75226760-C-A

24485947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75226990-C-T

24486303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75227220-G-A

24486331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75227242-G-A

24486621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75228005-G-A

24487018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75228392-A-G

24487031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 75228402-A-G

24487141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75228507-A-G

http://identifiers.org/hco/22/GRCh38#24487371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75228710-C-A

24487392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75228730-T-C

24487655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75228999-A-G

http://identifiers.org/hco/22/GRCh38#24487731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75229074-C-A

24487814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229157-G-A

24489025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229750-A-G

24489082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229806-G-A

http://identifiers.org/hco/22/GRCh38#24489096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#75229820-C-A

24489165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37122
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 75229881-T-C