http://identifiers.org/hco/17/GRCh38#69078758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110067608-C-A

69078758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110067608-C-T

69078850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110067686-A-T

69078869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110067698-C-G

http://identifiers.org/hco/17/GRCh38#69078939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110067766-A-C

69078945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110067772-T-C

69078945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110067772-T-G

69078947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110067774-A-G

69078960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 110067782-T-C

69078961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 110067783-A-G

http://identifiers.org/hco/17/GRCh38#69079022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110067844-A-C

69079038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110067860-T-G

69079110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110067920-A-G

69079124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110067934-T-C

69079140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110067953-G-A

69079140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110067953-G-T

http://identifiers.org/hco/17/GRCh38#69079153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110067967-C-A

69079153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110067967-C-T

69079180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110067980-G-T

69079300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110068094-T-C

69079309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110068103-T-C

69079470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110068344-T-C

69079471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110068345-A-G

69079504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110068373-G-A

69079504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110068373-G-T

69079601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110068454-A-G

69079683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110068534-C-T

69079750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110068602-A-G

69079843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110068694-T-C

69079904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110068755-A-G

69079937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110068814-G-A

69080052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110068925-C-T

69080456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069248-C-T

69080492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069271-G-A

69080542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069320-C-T

69080550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069328-G-A

69080555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069333-C-T

69080930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069490-C-T

69080969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069525-T-C

69080980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069536-A-G

69080983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069539-G-A

69080983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069539-G-T

69081015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069571-T-G

http://identifiers.org/hco/17/GRCh38#69081034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110069580-C-A

69081034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069580-C-T

http://identifiers.org/hco/17/GRCh38#69081135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110069667-A-C

69081135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110069667-A-G

69081154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069685-A-G

http://identifiers.org/hco/17/GRCh38#69081175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110069706-C-A

69081175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069706-C-T

69081216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110069729-G-T

69081586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110070105-C-G

http://identifiers.org/hco/17/GRCh38#69081844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110070248-A-C

69082023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110070384-T-G

69082024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110070385-T-C

69082178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110070536-T-C

69082283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110070638-G-A

69082326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110070682-C-G

http://identifiers.org/hco/17/GRCh38#69082328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110070684-A-C

69082328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110070684-A-G

http://identifiers.org/hco/17/GRCh38#69082342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110070698-C-A

69082386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110070750-C-G

69082386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110070750-C-T

69082394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110070758-C-T

69082635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110070889-T-C

69082707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110070914-G-T

69082709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110070916-G-A

69082841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110071021-C-T

69082916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110071096-T-C

69083028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110071215-G-C

69083093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110071276-A-G

http://identifiers.org/hco/17/GRCh38#69083106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110071290-C-A

69083106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110071290-C-T

69083117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110071301-A-G

69083198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110071341-G-A

http://identifiers.org/hco/17/GRCh38#69083259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110071402-C-A

69083259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110071402-C-T

69083295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110071438-T-C

69083337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110071480-G-A

69083418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110071582-A-G

69083451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110071610-T-C

69083909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110072268-G-A

69083915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110072274-T-C

69084147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110072479-A-G

69084234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110073646-G-A

69084250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110073663-A-G

69084299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110073712-T-A

69084299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110073712-T-C

http://identifiers.org/hco/17/GRCh38#69084344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110073757-C-A

http://identifiers.org/hco/17/GRCh38#69084394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110073815-A-C

69084443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110073864-T-C

69084524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110073945-T-C

69084770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110074189-T-C

69084866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110074716-G-A

69084866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110074716-G-T

http://identifiers.org/hco/17/GRCh38#69084883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110074733-C-A

69084883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110074733-C-T

69084913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110074763-A-G

69084913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110074763-A-T

http://identifiers.org/hco/17/GRCh38#69084946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#110074780-C-A

69084946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110074780-C-T

69084947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110074781-G-A

69084947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110074781-G-C

69084947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110074781-G-T

69084989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110074817-T-A

69084989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110074817-T-C

69084990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110074818-G-A

http://identifiers.org/hco/17/GRCh38#69084991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110074819-C-A

69084991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110074819-C-T

69085069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110074898-G-A

69085123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 110074952-G-A

69085123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 110074952-G-T

http://identifiers.org/hco/17/GRCh38#69085186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110075036-A-C

69085192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075041-T-A

69085192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075041-T-C

69085203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075052-T-G

69085239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075084-T-C

69085251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110075095-T-G

69085265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110075118-G-A

69085265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110075118-G-C

69085265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110075118-G-T

69085308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075161-T-C

69085324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075175-G-T

69085334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075182-T-A

69085386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075233-A-G

69085526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075369-A-G

69085568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075397-T-A

69085568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075397-T-C

69085568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075397-T-G

http://identifiers.org/hco/17/GRCh38#69085569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110075398-A-C

69085569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075398-A-G

http://identifiers.org/hco/17/GRCh38#69085576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110075405-A-C

69085576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075405-A-G

69085576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075405-A-T

http://identifiers.org/hco/17/GRCh38#69085611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110075443-C-A

69085646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110075482-G-T

69085703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110075539-T-A

69085742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075578-T-A

69085748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075584-A-G

69085748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075584-A-T

69085758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075594-C-T

http://identifiers.org/hco/17/GRCh38#69085781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110075613-C-A

69085781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075613-C-T

http://identifiers.org/hco/17/GRCh38#69085810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110075642-C-A

69085812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075644-T-C

http://identifiers.org/hco/17/GRCh38#69085845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110075675-A-C

69085845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075675-A-G

69085847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075677-G-A

69085883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075709-G-A

69085886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075712-A-T

69086084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075888-T-C

69086172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110075957-C-T

69086227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110076004-C-T

69086302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110076080-G-A

69086302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110076080-G-C

69086302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110076080-G-T

69086373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110076150-C-T

69086605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110077856-G-T

69086639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110077890-T-C

69086680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110077931-C-G

69086696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110077947-C-G

69086696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110077947-C-T

69086712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110077963-A-G

69086732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110077983-G-A

69086757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078008-T-C

69086757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078008-T-G

http://identifiers.org/hco/17/GRCh38#69086764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110078015-C-A

69086779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078029-C-T

69086801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078046-T-C

69086814-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078059-T-A

69086814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078059-T-C

69086907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078154-T-C

69087079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078435-G-T

http://identifiers.org/hco/17/GRCh38#69087256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110078571-C-A

69087256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078571-C-G

http://identifiers.org/hco/17/GRCh38#69087259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110078574-C-A

69087304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078627-A-G

69087365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110078682-T-G

69087450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110078767-G-A

69087492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110078806-G-A

69087492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110078806-G-C

69087546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110078848-G-A

69087546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110078848-G-T

69087548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110078850-G-A

69087548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110078850-G-T

69087574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110078876-T-A

69087574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110078876-T-C

69087636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078930-T-A

69087636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078930-T-C

69087636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078930-T-G

69087644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078938-G-A

69087644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078938-G-C

69087644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078938-G-T

http://identifiers.org/hco/17/GRCh38#69087658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110078952-C-A

69087658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078952-C-T

69087659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110078953-T-A

http://identifiers.org/hco/17/GRCh38#69087759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110079062-C-A

69087759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110079062-C-T

69087763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110079066-A-T

69087850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110079153-C-T

69087901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110079203-T-C

69088013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110079299-C-G

69088049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110079335-G-T

http://identifiers.org/hco/17/GRCh38#69088084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110079371-C-A

69088084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110079371-C-G

69088084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110079371-C-T

69088103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110079390-G-A

69088103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110079390-G-T

69088182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110079470-T-G

69088337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110079619-T-C

http://identifiers.org/hco/17/GRCh38#69088539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110079798-C-A

69088985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110080551-C-T

69089010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110080573-G-A

69089073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110080629-A-G

69089084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110080640-T-C

69089289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110080829-C-T

69089326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110080865-A-G

http://identifiers.org/hco/17/GRCh38#69089328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110080867-C-A

69089335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110080874-G-T

69089418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110080959-G-T

69089477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110081017-T-A

69089477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110081017-T-C

69089601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081128-G-A

69089601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081128-G-T

69089635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081158-T-C

69089680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081189-T-A

69089680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081189-T-G

69089781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081264-A-G

69089782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081265-T-A

69089909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081339-G-T

69089950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081381-G-A

69089950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081381-G-C

69090067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081498-T-A

69090067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081498-T-C

69090144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081570-T-C

69090213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081664-C-T

69090222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081675-C-T

http://identifiers.org/hco/17/GRCh38#69090355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110081778-C-A

69090355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081778-C-T

69090400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081823-C-G

69090423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110081846-T-C

69090639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110082056-A-G

69090696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110082088-A-T

69090704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110082096-T-C

69090743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110082135-G-A

69090867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110082254-G-A

69091276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110082577-T-A

69091348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110082604-G-T

69091430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110082682-C-T

http://identifiers.org/hco/17/GRCh38#69094596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110085546-C-A

69094596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110085546-C-T

69094652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110085606-T-C

69094731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110085672-A-G

69094787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110085726-A-T

69094842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110085777-G-T

http://identifiers.org/hco/17/GRCh38#69094899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110085834-C-A

69094899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110085834-C-G

69094915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110085849-C-T

http://identifiers.org/hco/17/GRCh38#69095004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110085936-C-A

69095004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110085936-C-T

http://identifiers.org/hco/17/GRCh38#69095067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110085988-C-A

69095067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110085988-C-T

69095098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110086019-G-A

69095098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110086019-G-T

69095151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110086072-A-G

69095151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110086072-A-T

69095186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110086119-G-A

69095186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110086119-G-T

69095282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110086194-A-G

http://identifiers.org/hco/17/GRCh38#69095322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110086218-C-A

69095322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110086218-C-T

69095341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110086237-T-G

69095401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110086290-T-A

69095401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110086290-T-C

69095424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110086313-G-T

69095516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110086381-T-C

69095646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110086441-G-A

69095813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110086724-T-A

69095813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110086724-T-C

69096010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110087056-C-T

69096060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110087107-C-T

69096188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110087338-A-T

69096216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110087471-T-C

69096348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110087627-T-A

69096348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110087627-T-C

http://identifiers.org/hco/17/GRCh38#69096379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110087652-A-C

69096379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110087652-A-G

http://identifiers.org/hco/17/GRCh38#69096419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110087685-C-A

69096423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110087689-T-C

http://identifiers.org/hco/17/GRCh38#69096494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110087719-C-A

69096494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110087719-C-T

http://identifiers.org/hco/17/GRCh38#69096591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110087797-A-C

69096591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110087797-A-G

69096610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110087816-A-G

69096676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110087880-T-C

69096712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110087916-A-G

69096714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110087918-T-C

69096793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110087997-A-G

69096836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110088030-A-T

69097421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110092622-G-A

69097421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110092622-G-T

http://identifiers.org/hco/17/GRCh38#69097535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110092734-A-C

69097535-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110092734-A-T

69097538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110092737-C-T

69097558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110092757-A-G

69097589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110092788-T-C

http://identifiers.org/hco/17/GRCh38#69097716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110092914-C-A

69097716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110092914-C-T

http://identifiers.org/hco/17/GRCh38#69097861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110093098-C-A

69097861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110093098-C-T

69097866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110093103-A-G

http://identifiers.org/hco/17/GRCh38#69097909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110093141-C-A

69097909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110093141-C-T

69097988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110093220-A-G

69098008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110093240-G-A

69098235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110093390-C-T

69098236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110093391-T-C

69098268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110093423-T-A

69098268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110093423-T-G

69098278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110093433-A-G

69098298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110093453-A-G

69098323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110093484-G-A

69098323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110093484-G-T

69098343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110093509-A-G

69098359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110093528-G-A

69098359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110093528-G-C

69098359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110093528-G-T

http://identifiers.org/hco/17/GRCh38#69098373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110093542-A-C

69098373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110093542-A-G

69098401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110093570-A-G

69098401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110093570-A-T

http://identifiers.org/hco/17/GRCh38#69100695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110099457-C-A

69100695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110099457-C-G

69100801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: 110099538-G-T

69100924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: 110099661-A-G

69100961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110099706-T-C

69100993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110099744-G-A

69100993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110099744-G-C

69100993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110099744-G-T

69101033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110099790-G-A

69101033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110099790-G-T

http://identifiers.org/hco/17/GRCh38#69101058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110099815-A-C

69101084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110099841-T-A

69101084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110099841-T-C

69101107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110099863-G-A

69101128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110099884-C-T

69101685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110100101-T-C

69101744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110100149-A-G

69101891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110100309-G-A

69101912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110100331-C-T

69101937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110100367-G-T

69102007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110100449-G-T

69102428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110100548-A-G

69102433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110100553-G-C

69102564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110100673-T-C

69102583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110100690-A-G

http://identifiers.org/hco/17/GRCh38#69102719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110100796-C-A

69102877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: synonymous variant
orthologous variants: 110100953-G-T

69103097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110101143-T-C

http://identifiers.org/hco/17/GRCh38#69103256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110101283-C-A

69103256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110101283-C-T

http://identifiers.org/hco/17/GRCh38#69103592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110101527-C-A

http://identifiers.org/hco/17/GRCh38#69104609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110101973-A-C

69104609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110101973-A-G

http://identifiers.org/hco/17/GRCh38#69104635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110101999-C-A

69104636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102000-A-G

69105031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102048-A-G

69105202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102259-A-G

69105202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102259-A-T

69105335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102376-G-A

69105335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102376-G-T

69105369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102400-T-G

69105378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102408-G-T

69105385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102415-T-A

69105385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102415-T-C

69105385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102415-T-G

69105407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102431-T-A

69105407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102431-T-C

69105407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102431-T-G

69105445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110102467-T-C

69105657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110102676-A-T

69105658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110102677-A-G

69105665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110102684-G-T

69105687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110102706-A-G

69105701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110102720-T-C

69105741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110102760-T-C

http://identifiers.org/hco/17/GRCh38#69105780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110102799-C-A

http://identifiers.org/hco/17/GRCh38#69105781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110102800-A-C

69105784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110102801-G-A

69105790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110102807-G-T

http://identifiers.org/hco/17/GRCh38#69105862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110102878-C-A

69105862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110102878-C-T

69105865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110102881-G-A

69105865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110102881-G-C

69105865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110102881-G-T

69106016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110103005-T-C

69106077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110103066-G-A

69106077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110103066-G-C

69106077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110103066-G-T

69106154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110103143-G-A

69106154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110103143-G-C

69106159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110103148-C-T

69106237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110103216-C-T

69106246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110103226-T-C

69106277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110103247-A-G

http://identifiers.org/hco/17/GRCh38#69106283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110103253-C-A

69106961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110103741-G-A

69106976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110103757-T-C

69107025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110103807-G-A

69107421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110104193-G-C

69107441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110104213-G-T

http://identifiers.org/hco/17/GRCh38#69107558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110104649-C-A

69107585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110104676-G-C

69107585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110104676-G-T

69107608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110104855-G-T

69107612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110104859-A-G

69107616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110104863-C-T

69107634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110104878-T-A

69107652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110104896-T-A

69107652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110104896-T-C

69107656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110104900-T-G

69107736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110104978-T-C

69107833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105075-T-C

69107833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105075-T-G

69107841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105083-T-A

http://identifiers.org/hco/17/GRCh38#69107850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110105092-C-A

http://identifiers.org/hco/17/GRCh38#69107867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110105110-C-A

69107875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105118-T-A

69107875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105118-T-C

69107971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105202-T-C

69107971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105202-T-G

http://identifiers.org/hco/17/GRCh38#69108034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110105258-C-A

69108034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105258-C-T

http://identifiers.org/hco/17/GRCh38#69108087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110105311-C-A

69108094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105318-A-T

http://identifiers.org/hco/17/GRCh38#69108096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110105320-C-A

69108118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105341-T-A

69108118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105341-T-C

69108128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105351-C-T

69108129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105352-G-A

69108129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105352-G-C

69108129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110105352-G-T

http://identifiers.org/hco/17/GRCh38#69110298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110106865-C-A

69110298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110106865-C-T

http://identifiers.org/hco/17/GRCh38#69110323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110106888-C-A

69110323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110106888-C-G

69110403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110106969-C-T

69110431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110106997-G-T

69110432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110106998-G-T

http://identifiers.org/hco/17/GRCh38#69110544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110107104-C-A

69110544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107104-C-T

http://identifiers.org/hco/17/GRCh38#69110545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110107105-C-A

69110545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107105-C-T

69110546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107106-A-T

http://identifiers.org/hco/17/GRCh38#69110623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110107180-C-A

69110623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107180-C-T

http://identifiers.org/hco/17/GRCh38#69110647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110107198-A-C

69110648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107199-A-G

69110653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107204-T-A

http://identifiers.org/hco/17/GRCh38#69110719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110107268-C-A

69110719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107268-C-G

69110719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107268-C-T

69110891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110107432-T-C

69110922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110107463-T-C

69110954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107495-G-T

69110956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107497-A-G

69110989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107560-T-A

69110989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107560-T-C

69111035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107604-T-C

69111035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107604-T-G

69111086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107650-A-G

69111086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107650-A-T

69111097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107661-T-C

69111097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107661-T-G

69111098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107662-G-A

69111098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107662-G-T

69111161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110107722-A-G

69112092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110108736-G-T

69112096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110108740-G-A

69112096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110108740-G-T

69112102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110108746-A-G

69112125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110108769-C-G

http://identifiers.org/hco/17/GRCh38#69112131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110108773-C-A

69112131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110108773-C-T

69112188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110109042-G-A

69112223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110109077-T-C

69112224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 110109078-A-G

http://identifiers.org/hco/17/GRCh38#69112256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110109110-A-C

69112335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109186-G-T

69112345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109208-G-A

69112345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109208-G-T

69112375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109235-T-C

http://identifiers.org/hco/17/GRCh38#69112394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110109254-A-C

69112394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109254-A-G

69112431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109291-A-T

69112435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109295-T-C

69112440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109300-G-A

69112440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109300-G-T

69112442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109302-A-G

69112871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109348-T-C

69112878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109355-A-G

http://identifiers.org/hco/17/GRCh38#69112887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110109364-C-A

69112994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109475-G-A

69112994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109475-G-C

69112994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109475-G-T

69113011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109488-T-A

69113094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109570-T-C

69113151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109618-C-T

69113185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109652-T-A

69113185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109652-T-C

69113206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109673-T-C

69113206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109673-T-G

69113368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 110109835-G-A

69113410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109875-T-C

69113429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109894-A-G

69113434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109899-A-G

69113535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109979-G-A

69113535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 110109979-G-T

69114586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110110194-A-G

69114593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110110201-A-G

http://identifiers.org/hco/17/GRCh38#69114681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110110287-A-C

69114682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110110288-A-G

http://identifiers.org/hco/17/GRCh38#69114690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110110295-A-C

69114739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110110344-T-A

69114773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110110377-C-T

69114983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110110595-A-G

69115022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110110634-A-T

69115164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110110709-C-T

69115174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110110719-T-A

69115174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110110719-T-C

69115308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110110834-G-A

69115308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110110834-G-C

69115308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110110834-G-T

69115340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110110868-A-G

69115399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110110927-T-A

http://identifiers.org/hco/17/GRCh38#69115521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110111037-C-A

69115521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110111037-C-T

69115562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110111079-T-C

69115657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110111170-T-C

69115662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110111174-C-T

69115663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110111175-A-G

69115700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110111212-G-A

69115700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110111212-G-C

69115700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110111212-G-T

http://identifiers.org/hco/17/GRCh38#69115732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110111234-C-A

http://identifiers.org/hco/17/GRCh38#69115774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110111274-A-C

69116317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110112197-T-C

69116317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110112197-T-G

69116332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110112212-A-G

69116341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110112221-C-T

69116407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110112271-C-T

69116482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110112345-T-C

69116501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 110112364-G-A

69116650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110112503-G-A

69116966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110113059-G-A

69117232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110113309-C-T

69117265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110113343-G-A

69117775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110121167-G-A

69117775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110121167-G-C

69117775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110121167-G-T

69117776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110121168-T-G

69117779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110121171-T-G

69117835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110121253-G-A

69117835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110121253-G-T

69117855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110121281-A-G

69117881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 110121298-T-C

69117910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110121327-C-G

69117910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 110121327-C-T

69117976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 110121392-G-T

http://identifiers.org/hco/17/GRCh38#69117990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110121408-C-A

69117990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110121408-C-T

http://identifiers.org/hco/17/GRCh38#69118044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110121454-C-A

69118044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110121454-C-T

69118074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110121483-G-A

69118074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110121483-G-T

69123197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110122842-G-A

69123197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110122842-G-T

69123225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110122867-A-G

69123304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: synonymous variant
orthologous variants: 110122946-A-G

http://identifiers.org/hco/17/GRCh38#69123340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110122982-C-A

69123340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: 110122982-C-G

69123579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110123191-G-T

69123641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110123244-A-G

http://identifiers.org/hco/17/GRCh38#69123942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110123280-A-C

69123956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110123294-A-G

69124394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110123721-T-G

69124439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110123769-T-C

http://identifiers.org/hco/17/GRCh38#69124748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110124321-C-A

69124847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110124483-T-A

69124847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110124483-T-C

http://identifiers.org/hco/17/GRCh38#69124922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110124555-C-A

69124922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: 110124555-C-G

69124922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: synonymous variant
orthologous variants: 110124555-C-T

http://identifiers.org/hco/17/GRCh38#69124983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110124616-C-A

69125021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: synonymous variant
orthologous variants: 110124654-A-G

69125053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110124690-A-G

69125063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110124700-T-A

69125063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110124700-T-C

69125063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110124700-T-G

69125064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110124701-T-A

69125078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110124710-T-A

69125107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110124737-T-C

69125108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110124738-T-A

69125108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110124738-T-C

69125124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110124754-T-C

69125147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110124783-T-C

69125150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110124786-T-C

69128476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127308-T-G

69128510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127334-A-G

http://identifiers.org/hco/17/GRCh38#69128511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110127335-A-C

69128525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127349-A-T

69128541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127366-G-T

69128555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127380-A-T

69128558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127383-G-T

69128566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127392-A-T

69128567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127393-G-A

69128567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127393-G-T

69128581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127407-T-C

69128588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127414-T-C

69128609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127427-A-G

http://identifiers.org/hco/17/GRCh38#69128681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110127499-A-C

http://identifiers.org/hco/17/GRCh38#69128796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110127614-C-A

69128832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127647-T-A

69128832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127647-T-C

69128835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127650-T-A

69128835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127650-T-C

69128899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127687-A-G

69129033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127807-G-A

69129144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127916-G-A

69129186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110127961-G-T

69129415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110132143-G-C

69129529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110132290-G-C

69129561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110132312-A-G

69129655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: synonymous variant
orthologous variants: 110132406-G-T

69129675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: stop gained
orthologous variants: 110132426-G-A

69129783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110132532-G-A

69129783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110132532-G-T

69129884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110132635-T-C

69130476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110132935-T-C

69130527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110132990-T-C

69130552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110133015-A-G

http://identifiers.org/hco/17/GRCh38#69130581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110133039-A-C

69130700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110133180-C-T

69130958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110133431-C-T

69131102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110133569-G-A

69131208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110133670-T-C

69132365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110134225-T-C

69132963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110134393-C-T

69133060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110134470-C-G

69133129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110134530-A-G

69133237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110134622-A-G

69133417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110134800-A-G

69133435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110134818-C-T

http://identifiers.org/hco/17/GRCh38#69133521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110134901-C-A

69133521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110134901-C-T

69133539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110134918-A-G

69133562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110134941-G-A

69133562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110134941-G-T

69133577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110134956-C-T

69133739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: synonymous variant
orthologous variants: 110135091-G-A

http://identifiers.org/hco/17/GRCh38#69133885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110135237-C-A

69133885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110135237-C-G

69133885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110135237-C-T

http://identifiers.org/hco/17/GRCh38#69133923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110135269-C-A

http://identifiers.org/hco/17/GRCh38#69133975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110135323-C-A

69133975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110135323-C-G

69134108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110135461-T-C

http://identifiers.org/hco/17/GRCh38#69134315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110135681-C-A

69134353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110135724-G-T

69134421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110135837-T-C

69134596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110136001-G-A

69134602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110136007-G-C

69134602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110136007-G-T

69134616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110136021-G-T

69134628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110136033-C-T

69134675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: synonymous variant
orthologous variants: 110136080-C-T

69134714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: synonymous variant
orthologous variants: 110136119-A-G

69134726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: synonymous variant
orthologous variants: 110136131-T-C

69134833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110136238-G-T

http://identifiers.org/hco/17/GRCh38#69134841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110136246-A-C

69134845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110136251-G-A

69134845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110136251-G-C

69134845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110136251-G-T

69135346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137477-G-C

http://identifiers.org/hco/17/GRCh38#69135372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110137503-C-A

69135372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137503-C-G

69135398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137533-T-C

http://identifiers.org/hco/17/GRCh38#69135401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110137536-C-A

69135401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137536-C-T

69135443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137578-G-A

69135459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137594-T-A

http://identifiers.org/hco/17/GRCh38#69135483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110137617-C-A

69135483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137617-C-G

69135483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137617-C-T

69135507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137644-T-C

http://identifiers.org/hco/17/GRCh38#69135528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110137669-C-A

69135609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137711-T-C

http://identifiers.org/hco/17/GRCh38#69135793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110137865-C-A

69135793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137865-C-T

http://identifiers.org/hco/17/GRCh38#69135797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110137869-C-A

69135812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137885-G-A

69135812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137885-G-T

http://identifiers.org/hco/17/GRCh38#69135835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110137908-C-A

69135835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137908-C-T

http://identifiers.org/hco/17/GRCh38#69135895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110137948-A-C

69135895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137948-A-G

69135895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137948-A-T

69135897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 110137950-G-T

69136041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, missense_variant
orthologous variants: 110138040-T-C

69136041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, missense_variant
orthologous variants: 110138040-T-G

69136061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron_variant, missense_variant
orthologous variants: 110138060-T-A

http://identifiers.org/hco/17/GRCh38#69136108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110138108-C-A

http://identifiers.org/hco/17/GRCh38#69136209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/11/GRCm39#110138209-C-A

69136209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: 110138209-C-T

69136312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110138318-T-C

69136313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110138319-G-T

69136324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110138330-G-A

69136324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110138330-G-C

69136324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110138330-G-T

69136326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110138332-T-C

69136453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110138429-T-C

69136836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110138733-T-A

69137110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110138995-G-T

69137186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110139065-T-A

69137186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110139065-T-C

http://identifiers.org/hco/17/GRCh38#69137369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110139245-C-A

69137369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: 110139245-C-G

69137369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: 110139245-C-T

69137426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: synonymous variant
orthologous variants: 110139302-A-G

69137485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: 110139361-T-C

69137514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110139394-A-G

69137565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110139442-T-C

http://identifiers.org/hco/17/GRCh38#69137567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110139444-C-A

69137567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110139444-C-T

http://identifiers.org/hco/17/GRCh38#69137599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110139475-C-A

69137599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110139475-C-T

69137683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110139558-T-C

69137729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110139596-A-T

69137807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110139673-T-C

69140184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110140805-C-G

69140248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110140850-G-A

69140540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110141159-G-T

http://identifiers.org/hco/17/GRCh38#69140561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110141181-C-A

69140561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110141181-C-G

69140561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110141181-C-T

69140562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110141182-A-G

69140614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: 110141230-G-C

69140614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: 110141230-G-T

http://identifiers.org/hco/17/GRCh38#69140682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110141298-C-A

69140682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: missense variant
orthologous variants: 110141298-C-T

69140707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 5 prime UTR variant
orthologous variants: 110141329-G-T

69140722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 5 prime UTR variant
orthologous variants: 110141344-G-A

69140722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 5 prime UTR variant
orthologous variants: 110141344-G-T

69140728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 5 prime UTR variant
orthologous variants: 110141350-G-A

69140728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 5 prime UTR variant
orthologous variants: 110141350-G-T

http://identifiers.org/hco/17/GRCh38#69140748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110141364-C-A

69140748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 110141364-C-T

69140780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110141387-T-C

69140999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110141605-A-T

69141073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110141668-T-C

69141231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110141818-G-C

69141693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: intron variant
orthologous variants: 110142343-C-T

69141765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 5 prime UTR variant
orthologous variants: 110142413-G-T

69141856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 5 prime UTR variant
orthologous variants: 110142492-T-C

http://identifiers.org/hco/17/GRCh38#69141862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#110142498-C-A

69141871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 36
most severe consequence: 5 prime UTR variant
orthologous variants: 110142508-G-A