http://identifiers.org/hco/10/GRCh38#94402762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38825293-A-C

94403049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38825487-T-A

94403049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38825487-T-C

94403163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38825568-G-A

94403163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38825568-G-C

94403163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 38825568-G-T

94403344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38825662-A-G

94403344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38825662-A-T

94403386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38825692-G-A

94403386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38825692-G-C

94403386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38825692-G-T

94403486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 38825792-G-A

http://identifiers.org/hco/10/GRCh38#94403722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38825966-C-A

94403722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38825966-C-T

94403879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38826079-G-A

94403879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38826079-G-C

94403890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38826090-T-A

94404227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38826873-G-A

94404746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38827470-G-A

94405322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38828148-A-G

94405373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38828195-G-C

94405540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38828543-G-A

http://identifiers.org/hco/10/GRCh38#94405626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38828605-A-C

94405679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38828656-G-C

94405992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38829024-G-T

94406001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38829033-A-G

94406378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38829343-A-G

http://identifiers.org/hco/10/GRCh38#94406398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38829363-A-C

94406398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38829363-A-G

94406399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38829364-G-C

94406645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38829602-A-G

http://identifiers.org/hco/10/GRCh38#94406651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38829608-C-A

94406711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38829859-A-G

http://identifiers.org/hco/10/GRCh38#94406718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38829866-A-C

94406718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38829866-A-G

94406759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38829964-G-A

94406759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38829964-G-T

94410945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38832481-C-T

94410947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38832483-C-G

94413052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38834626-A-G

94413596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38835092-C-G

94414235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38836320-C-T

94414255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38836340-T-C

94414256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38836341-G-C

94414264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38836349-G-A

http://identifiers.org/hco/10/GRCh38#94414318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38836401-A-C

94414341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38836424-G-T

94414376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38836458-A-G

94414457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38836556-T-C

94414492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38836589-T-C

94414993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38837377-G-A

http://identifiers.org/hco/10/GRCh38#94415137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38837511-C-A

94417518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38841438-A-G

94417518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38841438-A-T

94417609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38841510-C-T

94427688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842706-C-T

94427724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842741-T-C

94427774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842782-G-A

94427795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842801-G-T

http://identifiers.org/hco/10/GRCh38#94427823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38842824-C-A

94427848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842852-A-T

94427858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842862-G-A

94427859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842863-G-A

94427859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842863-G-T

94427863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842867-G-A

94427863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842867-G-T

94427867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38842871-A-G

http://identifiers.org/hco/10/GRCh38#94427885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38842879-A-C

94428284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38843400-T-C

94428889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38843939-G-A

94429290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844403-C-G

94429290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844403-C-T

94429300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38844413-A-T

http://identifiers.org/hco/10/GRCh38#94429506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#38844629-C-A

94429602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 38844707-T-C

http://identifiers.org/hco/10/GRCh38#94441283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38853065-A-C

94441757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38853923-A-G

94441757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38853923-A-T

94441865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38854031-A-G

http://identifiers.org/hco/10/GRCh38#94442789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38855113-C-A

94442898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38855209-T-C

94444524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38857051-C-G

94446373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38857601-A-G

94446393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38857620-T-G

94446515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38863577-T-G

94447093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38863733-T-C

94447380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38864359-A-G

94447427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38864408-A-G

http://identifiers.org/hco/10/GRCh38#94447469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38864450-C-A

94447524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38864561-A-T

94447568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38864608-A-G

94447620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38864660-T-C

http://identifiers.org/hco/10/GRCh38#94447707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38864735-A-C

94447707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38864735-A-T

94447829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38864847-T-A

94447876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38864893-C-G

94448095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38865349-C-T

94448414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38865702-A-G

94448959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38865915-T-C

94449343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38866264-C-T

94450477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38867342-T-C

http://identifiers.org/hco/10/GRCh38#94473585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38869882-A-C

94473631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38869989-T-G

94474003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38870596-T-G

94474202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38870834-A-G

94474552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38871002-A-G

94474552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38871002-A-T

94474588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38871021-A-G

94474604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38871037-A-G

94474775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38871210-T-C

94474865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38871308-G-A

94474865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38871308-G-C

94474868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38871311-A-G

94474928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38871437-C-T

94475187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38871847-C-G

94476466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38874072-C-T

94476576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38874182-T-C

94476576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38874182-T-G

94476631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38874225-T-G

94476674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38874264-C-T

94477028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38876275-G-T

94477264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38876489-T-C

94477372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38876592-G-A

94477408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38876629-A-G

94477534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38876730-C-G

94477534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38876730-C-T

94490879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38881211-G-T

94490961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38881275-C-T

94491116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38881422-C-T

94491428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38881834-A-G

94493145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38884135-T-C

94493190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38884185-C-T

94493241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38884236-C-T

94493333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38884405-A-G

94493818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38884834-A-G

94493835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38884851-T-C

http://identifiers.org/hco/10/GRCh38#94494060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38885046-C-A

94494060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38885046-C-G

94494437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38885442-G-C

94494437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38885442-G-T

http://identifiers.org/hco/10/GRCh38#94497392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38887528-C-A

94499843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38889377-C-G

http://identifiers.org/hco/10/GRCh38#94500000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38889554-C-A

94500078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38889617-A-G

94500083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38889622-A-G

94500087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38889626-A-G

94500090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38889629-A-G

94500090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38889629-A-T

94500093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38889632-T-A

94500093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38889632-T-G

94500108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38889647-A-G

94500108-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38889647-A-T

94500170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38889702-T-C

94500365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38889895-A-G

94504578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38893481-T-A

94504682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38893575-A-T

94504725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38893638-G-A

94504782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38893694-G-C

94504911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38893822-T-C

94506928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38895704-G-T

94507052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38895822-T-C

94507117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38895900-G-T

http://identifiers.org/hco/10/GRCh38#94507130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38895914-A-C

94507151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38895939-G-T

94507161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38895950-A-G

94507161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38895950-A-T

http://identifiers.org/hco/10/GRCh38#94509884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38898662-C-A

94509884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38898662-C-G

94509884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38898662-C-T

94510067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 38899428-A-G

94510292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38900290-T-C

94510295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38900301-G-A

94510295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38900301-G-C

94511539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38901588-G-A

94511539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38901588-G-T

94511684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38901736-A-G

94511695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38901747-T-A

94511695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38901747-T-C

94511740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38901781-A-G

http://identifiers.org/hco/10/GRCh38#94511803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38901842-C-A

94511803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38901842-C-G

94511803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38901842-C-T

http://identifiers.org/hco/10/GRCh38#94521884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38902316-A-C

http://identifiers.org/hco/10/GRCh38#94521981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38902399-A-C

94521981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38902399-A-G

94522047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38902465-A-G

94522047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38902465-A-T

94522272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38902682-G-A

94522272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38902682-G-T

94522334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38902738-T-G

http://identifiers.org/hco/10/GRCh38#94522389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38902793-C-A

94522389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 38902793-C-G

94522389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 38902793-C-T

http://identifiers.org/hco/10/GRCh38#94522417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38902821-C-A

94522417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 38902821-C-T

94522418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38902822-T-A

94522418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38902822-T-C

94522418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 38902822-T-G

94522467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38902872-T-C

94522507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38902909-T-G

94522663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38903051-G-A

94522663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38903051-G-C

94522663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38903051-G-T

94531496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38905357-T-C

94532881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38906213-A-T

94533018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38906305-T-C

http://identifiers.org/hco/10/GRCh38#94533083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38906370-C-A

94533083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38906370-C-T

http://identifiers.org/hco/10/GRCh38#94533102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38906389-A-C

94533124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38906409-T-A

94533124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38906409-T-C

94533142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38906427-G-A

94533142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38906427-G-T

94533212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38906488-G-A

94533212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38906488-G-T

http://identifiers.org/hco/10/GRCh38#94533220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38906497-A-C

94533220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38906497-A-G

http://identifiers.org/hco/10/GRCh38#94533221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#38906498-C-A

94533221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38906498-C-T

94533237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38906514-T-A

94533237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38906514-T-C

94533258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 38906535-T-C

94533483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3 prime UTR variant
orthologous variants: 38906765-G-A

94533630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3 prime UTR variant
orthologous variants: 38906910-C-T

94535325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38907507-C-G

94535469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38907669-A-G

94535584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29082
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 38907776-G-A