134432844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21656122-A-G

134432861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21656108-T-C

134432872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21656097-A-T

134433106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21655866-A-G

134433134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21655838-G-A

134433134-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21655838-G-C

134433134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21655838-G-T

134433260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21655712-C-G

134435574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21653201-G-A

http://identifiers.org/hco/6/GRCh38#134435712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21653072-A-C

134435962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21652888-A-T

134435993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21652857-A-G

134436477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21652437-C-T

134436518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21652402-C-G

134436524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21652396-A-G

134436569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21652351-T-A

134436690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21652232-C-T

134436988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21651965-C-T

134437158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21651802-T-C

134437500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21651482-C-T

http://identifiers.org/hco/6/GRCh38#134437591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21651413-C-A

134437682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21651327-G-T

134437737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21651277-G-T

134437821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21651190-G-A

134437821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21651190-G-T

134437989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21651029-G-A

134437989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21651029-G-T

134438075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21650871-T-C

134438245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21650711-G-A

134438245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21650711-G-C

134438279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21650677-T-C

134438343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21650630-G-A

134438419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21650560-C-T

134439167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21650095-T-G

134439542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21644305-G-A

134439644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21644201-T-C

134441497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21643440-A-G

134441502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21643435-A-T

134441644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21643298-G-A

134441655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21643286-C-T

http://identifiers.org/hco/6/GRCh38#134441688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21643257-A-C

134441699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21643246-G-C

134442633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642177-T-G

134442664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642147-G-C

134442677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21642143-T-C

134444648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21640159-G-C

134446418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638970-C-T

134446523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638865-T-A

http://identifiers.org/hco/6/GRCh38#134446535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21638853-C-A

134446692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638688-G-A

134447238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638163-C-G

134447242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638159-C-T

134447252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638147-A-G

134447351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638057-G-A

134447352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21638056-T-A

http://identifiers.org/hco/6/GRCh38#134448039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#21636815-C-A

134448046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21636808-C-G

http://identifiers.org/hco/6/GRCh38#134448058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#21636796-A-C

134448063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21636791-T-A

134448428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21636462-G-A

134448432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21636458-G-A

http://identifiers.org/hco/6/GRCh38#134448527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21636357-A-C

134448527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21636357-A-G

134448527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21636357-A-T

134448687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21636203-A-G

http://identifiers.org/hco/6/GRCh38#134449008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21635660-A-C

134449008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21635660-A-T

134449037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21635634-C-T

134449067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21635604-C-G

134449649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21634934-C-T

http://identifiers.org/hco/6/GRCh38#134449655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21634928-C-A

134449655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21634928-C-T

134449659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21634924-C-T

134449919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21634454-G-A

134449931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21634442-C-T

134450061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21634290-C-T

134450215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21634170-G-A

134450426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21633975-A-T

134450465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21633937-G-A

134450465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21633937-G-T

134450541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21633859-G-A

134450561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21633839-G-A

134450730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21633667-A-G

http://identifiers.org/hco/6/GRCh38#134450940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21633398-C-A

134450940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21633398-C-T

134453295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21633264-G-A

134453376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21633195-G-A

134453475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21633096-C-T

http://identifiers.org/hco/6/GRCh38#134453617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21632953-C-A

134453686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21632878-G-C

134453714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21632849-T-A

134454168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21631921-G-A

134454168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21631921-G-C

134454168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21631921-G-T

134454213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21631876-G-A

134454254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21631835-T-G

134454257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21631832-A-G

134454344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21631761-A-G

134454469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21631655-G-T

http://identifiers.org/hco/6/GRCh38#134454488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21631636-C-A

134454778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21631389-A-G

134454898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21631285-C-T

134454919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21631264-T-C

134454920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21631263-A-G

134455520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21631016-C-T

134455587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21630961-T-C

134456012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21630391-T-C

134456053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21630320-A-G

134456361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21629986-C-T

134456381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21629966-T-C

134457456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21628355-A-G

134457564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21628258-G-A

http://identifiers.org/hco/6/GRCh38#134457821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21627754-C-A

134457821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21627754-C-T

134457831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21627745-T-C

134458003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21627619-T-C

134458138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21627489-G-T

134458140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21627487-C-T

134458147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21627478-T-C

http://identifiers.org/hco/6/GRCh38#134458176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21627449-C-A

134458176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21627449-C-T

134458231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21627399-G-A

http://identifiers.org/hco/6/GRCh38#134458612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21626499-C-A

134458612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21626499-C-G

134458612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21626499-C-T

134458665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21626458-T-C

134458717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21626397-G-A

134458817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21626321-C-T

134458819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21626319-T-C

134458851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21626278-G-A

134458851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21626278-G-C

134459115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21625987-A-G

134459127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21625976-G-C

134459127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21625976-G-T

134459144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21625959-C-G

134459174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21625930-C-T

134459245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21625891-C-T

134461960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21623802-A-G

134464795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21622967-A-G

134464922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21622852-G-A

134465759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21622429-C-T

134465827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21622367-A-T

134465843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21622360-T-A

134466137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21622101-G-A

134466141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21622097-C-G

134466141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21622097-C-T

134466262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21621981-T-C

134466380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21621870-T-G

134466388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21621844-T-C

http://identifiers.org/hco/6/GRCh38#134466472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21621773-C-A

134467197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21620965-T-C

http://identifiers.org/hco/6/GRCh38#134467516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21620711-C-A

134467516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620711-C-T

134467758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620610-G-A

134467807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21620563-G-T

http://identifiers.org/hco/6/GRCh38#134467842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21620525-C-A

134467935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21620434-T-C

134468187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21620118-C-G

134468489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21619794-G-T

134468647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21619633-G-C

http://identifiers.org/hco/6/GRCh38#134468667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21619614-C-A

134468695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21619590-C-T

134468743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21619545-A-G

134469160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21619155-G-A

134469175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21619140-T-C

134469345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618988-C-T

134469578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618758-C-T

134469643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618695-C-T

134469825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618573-T-C

134469908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618489-G-A

134469911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618486-C-T

134470059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618332-G-A

134470059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618332-G-T

134470116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618276-A-G

134470229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618161-T-C

134470238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618152-G-A

134470251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618139-G-A

134470255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618134-G-A

134470372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21618017-C-T

134470631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617773-A-G

http://identifiers.org/hco/6/GRCh38#134470658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21617747-A-C

134472296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617033-T-C

134472303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21617026-G-T

134472546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616642-G-T

134472560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616628-A-T

134472706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616510-G-A

134472887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616331-A-G

134472904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616314-A-G

134473128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616096-T-C

134473128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616096-T-G

134473160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21616064-G-C

http://identifiers.org/hco/6/GRCh38#134474454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21615693-A-C

http://identifiers.org/hco/6/GRCh38#134474481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21615665-A-C

134474481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21615665-A-T

134478043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21614013-T-G

134478158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21613907-A-G

134478467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21613610-C-G

134478469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21613608-A-G

http://identifiers.org/hco/6/GRCh38#134480891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21603274-C-A

134482142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21601964-T-C

134482150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21601956-C-T

134482182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21601924-A-G

134482268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21601839-T-G

134482279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21601828-C-T

134482286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21601821-C-T

134483026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600524-G-A

134483132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600445-G-A

134483132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600445-G-T

134483204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600358-A-T

134483205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600357-G-A

134483311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21600236-T-C

134485452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598811-T-A

134485452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598811-T-G

134485457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598806-G-C

134485468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21598795-T-C

134495908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21594811-G-A

134496086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21594638-A-G

134496920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21594460-G-C

134496920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21594460-G-T

134497074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21594313-G-A

134497457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21593937-C-G

134497457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21593937-C-T

http://identifiers.org/hco/6/GRCh38#134497609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21593782-A-C

134498035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21593708-G-A

134498057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21593676-C-T

134498495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21593250-G-A

134498495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21593250-G-C

134498507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21593239-G-A

134498528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21593218-G-C

134500193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21591439-G-A

http://identifiers.org/hco/6/GRCh38#134500364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21591242-C-A

134500569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21591063-G-A

134501054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21590955-G-A

134501055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21590954-G-C

134501094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21590908-T-A

134501340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21590760-A-G

134501428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21590674-A-G

134501532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21590586-A-T

http://identifiers.org/hco/6/GRCh38#134501626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21590507-C-A

134502039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21590427-A-G

134502572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21589086-C-T

134502605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21589054-T-C

134502699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21588946-A-T

134502867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588896-A-G

134502895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588868-G-T

134502901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588862-G-A

134502984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588796-A-G

http://identifiers.org/hco/6/GRCh38#134502999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21588781-C-A

134502999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588781-C-G

134502999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588781-C-T

134503068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 21588721-G-C

http://identifiers.org/hco/6/GRCh38#134503111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21588687-C-A

134503111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588687-C-T

134503152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588650-A-G

134503167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588635-A-G

134503168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588634-G-A

134503168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588634-G-T

134503200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588606-G-T

134503240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588571-G-T

134503241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588570-A-G

134503241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588570-A-T

134503243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588568-G-T

134503246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588565-T-G

134503275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588536-G-A

134503275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588536-G-T

http://identifiers.org/hco/6/GRCh38#134503309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21588504-C-A

134503316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588497-G-T

134503349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588464-G-T

http://identifiers.org/hco/6/GRCh38#134503361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21588457-C-A

134503376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588440-T-C

http://identifiers.org/hco/6/GRCh38#134503395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21588421-C-A

134503395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588421-C-T

http://identifiers.org/hco/6/GRCh38#134503399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21588417-C-A

134503417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588411-G-T

134503419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588409-G-C

134503419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588409-G-T

134503443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588393-A-G

134503443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588393-A-T

134503489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588348-G-T

http://identifiers.org/hco/6/GRCh38#134503673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21588107-C-A

http://identifiers.org/hco/6/GRCh38#134503714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21588028-C-A

134503728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588014-C-T

134503742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21588000-G-T

134503762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21587975-C-G

134503930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21587808-T-C

134503943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21587796-T-C

134504078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21587667-T-C

134504267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21587479-A-G

134504319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21587426-T-A

134504319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21587426-T-C

134504404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21587324-C-T

134504448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21587282-A-G

134505089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21587050-A-G

134505185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21586980-T-C

http://identifiers.org/hco/6/GRCh38#134505285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21586913-A-C

134505430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21586768-G-T

http://identifiers.org/hco/6/GRCh38#134505662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21586556-C-A

134505735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21586478-C-T

134505792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21586384-T-C

134506095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21585701-A-G

134506606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21585215-T-C

134506606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21585215-T-G

http://identifiers.org/hco/6/GRCh38#134506626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21585195-A-C

134506828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21585007-T-C

134507152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21584663-T-A

134509262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

134509290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

134509290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-C

134509290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

134509358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

134509396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

134509426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

134509468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

134509576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/6/GRCh38#134509577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

134509760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21580800-T-G

134509911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21580674-C-T

134509990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21580599-G-A

134510019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21580572-A-G

134510206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21580393-T-C

134510243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21580352-C-T

http://identifiers.org/hco/6/GRCh38#134510248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21580347-A-C

134510428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21580168-C-T

134510750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21580130-A-G

http://identifiers.org/hco/6/GRCh38#134510886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21580013-C-A

134510946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21579926-T-C

134511007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21579864-A-T

134511048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21579823-C-T

134511168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21579706-T-A

134511186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21579689-A-G

134511396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 21579491-T-C

134511537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21578756-G-A

134511537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21578756-G-C

134511754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21578578-A-G

134512715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21577981-C-T

134512754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21577942-T-C

134513103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21577590-A-G

http://identifiers.org/hco/6/GRCh38#134513156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21577535-C-A

134513168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21577523-C-T

134513205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21577487-C-G

134513324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21577394-C-T

134513400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21577328-G-A

134514052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21576671-G-A

134514057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21576666-A-T

134514609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21576256-G-A

134514846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21576034-T-C

134514884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21576002-A-T

134515259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21575594-G-A

134515362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21575476-A-T

134515377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21575461-C-T

http://identifiers.org/hco/6/GRCh38#134515464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21575353-A-C

http://identifiers.org/hco/6/GRCh38#134515758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21575108-A-C

134515761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21575105-T-C

134516039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21574851-T-C

134516110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21574797-T-C

134516110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21574797-T-G

http://identifiers.org/hco/6/GRCh38#134516162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21574745-A-C

134516307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21574627-A-T

134516318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21574615-G-A

http://identifiers.org/hco/6/GRCh38#134516814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21574238-A-C

134516842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21574211-C-T

134516850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21574203-G-A

134517367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21573719-A-G

http://identifiers.org/hco/6/GRCh38#134517630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21573491-A-C

134517630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21573491-A-T

http://identifiers.org/hco/6/GRCh38#134517828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#21573114-A-C

134517853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21573090-C-T

134517874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21573069-G-T

134517878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21573065-C-T

134517927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21573016-G-C

134518015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21572996-G-A

134518122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21572909-G-A

134518243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21572701-T-G

134518256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21572688-A-G

134518397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21572563-G-A

134518785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21572280-C-T

134520047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21570940-C-T

134520094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21570893-G-C

134520094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37196
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21570893-G-T