http://identifiers.org/hco/5/GRCh38#81312740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91945178-C-A

81312740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91945178-C-T

81312761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91945157-G-A

81312761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91945157-G-T

81312769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91945149-T-C

http://identifiers.org/hco/5/GRCh38#81312829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91944997-C-A

81312868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91944926-G-A

81312879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91944915-G-T

http://identifiers.org/hco/5/GRCh38#81312914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91944881-C-A

81312933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91944862-T-C

http://identifiers.org/hco/5/GRCh38#81313213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91944620-C-A

81313299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91944527-A-G

http://identifiers.org/hco/5/GRCh38#81326645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91937559-A-C

http://identifiers.org/hco/5/GRCh38#81326933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91937322-C-A

81326971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91937288-T-C

81327092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91937212-G-A

81327107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91937197-T-C

81327266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91936974-A-G

81327298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91936944-T-C

81327301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91936941-T-C

81327814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91936749-G-A

81328004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91935974-T-C

81328005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91935973-G-A

http://identifiers.org/hco/5/GRCh38#81329299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91933894-C-A

http://identifiers.org/hco/5/GRCh38#81329614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91933609-C-A

81329773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91933451-T-C

http://identifiers.org/hco/5/GRCh38#81329883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91933336-A-C

81329976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91933246-A-G

http://identifiers.org/hco/5/GRCh38#81330043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91933195-C-A

81330095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 91933143-T-A

http://identifiers.org/hco/5/GRCh38#81330107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91933131-A-C

81330107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 91933131-A-G

81330187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 91933083-T-C

http://identifiers.org/hco/5/GRCh38#81330189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91933081-C-A

81330189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 91933081-C-T

81330204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 91933067-G-C

81330204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 91933067-G-T

81330225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 91933046-A-G

81330291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 91932989-A-T

81330378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91932914-A-G

81330533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91932758-A-G

81330536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91932755-T-C

81330740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91932599-A-G

http://identifiers.org/hco/5/GRCh38#81330818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91932520-C-A

81330818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91932520-C-T

81330878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91932460-T-C

81330878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91932460-T-G

81330890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91932448-G-A

http://identifiers.org/hco/5/GRCh38#81330953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91932380-A-C

81330953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91932380-A-G

http://identifiers.org/hco/5/GRCh38#81330982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91932361-A-C

81331169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91932237-A-G

81331343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91932111-T-A

81331397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91932103-C-G

http://identifiers.org/hco/5/GRCh38#81331690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91931907-C-A

81332008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931598-G-A

81332009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931597-A-T

81332184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931433-G-A

81332228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931388-C-G

81332228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931388-C-T

81332231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931384-G-A

81332334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931291-T-C

81332334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931291-T-G

81332383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931236-A-G

81332386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931233-T-A

http://identifiers.org/hco/5/GRCh38#81332390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91931229-C-A

81332390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931229-C-T

http://identifiers.org/hco/5/GRCh38#81332392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91931227-C-A

81332408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931211-C-T

81332416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931206-C-G

81332416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931206-C-T

81332425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931197-T-C

81332435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931187-A-G

81332435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91931187-A-T

http://identifiers.org/hco/5/GRCh38#81332475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91931147-A-C

81332476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 91931146-C-T

81332659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930966-C-G

81332659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930966-C-T

81332660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930965-A-G

81332682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930943-A-G

81332690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930935-A-G

81332691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930934-T-A

81332691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930934-T-C

81333225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930718-T-C

81333271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930683-A-G

81333337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930620-T-G

81333372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930588-T-G

81333435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930517-T-G

81333447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930505-C-T

http://identifiers.org/hco/5/GRCh38#81333537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91930409-C-A

81333551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930395-C-T

81333555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91930391-T-A

http://identifiers.org/hco/5/GRCh38#81335676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91929525-C-A

81335676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91929525-C-T

81335724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91929482-T-C

81335727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91929479-T-A

81335727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91929479-T-C

http://identifiers.org/hco/5/GRCh38#81335731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91929475-A-C

81335739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91929467-T-C

81335741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91929465-G-A

81335904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 91929301-A-G

81335997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91929153-T-A

81335997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91929153-T-C

81336106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91929086-A-G

81336109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91929083-C-T

81336259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91928952-T-A

81336560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91928724-T-G

81336684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91928369-T-A

81336744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91928309-T-C

81336927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91928107-G-T

81337184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91927929-T-C

81337239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91927883-G-A

81337351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91927799-T-G

81337495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91927670-C-G

81337634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91927546-C-T

81337735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91927459-A-T

81337768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91927426-A-G

81339163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91926465-C-G

81339307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91926334-A-G

81339399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91926254-A-G

81339414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91926242-C-T

81339457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91926206-C-T

81339485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91926181-C-G

81339486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91926180-A-G

81339739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91925958-T-C

81339752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91925945-T-A

81339848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91925852-C-G

81341127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91924746-A-T

81341158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91924605-A-G

81341635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91924148-C-G

81341635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91924148-C-T

81341713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91924069-T-A

81341788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91924006-T-C

http://identifiers.org/hco/5/GRCh38#81342453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91923234-C-A

81342541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91923162-T-C

81342619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91923081-A-G

81342639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91923061-G-A

81342639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91923061-G-C

81342646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91923055-T-C

81342659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91923043-G-T

81342787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91922919-T-C

81342792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91922914-T-C

81342792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91922914-T-G

81342807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91922899-G-A

81342867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91922835-T-A

81343559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91921176-A-G

81343669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91921083-G-A

81343669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91921083-G-T

81343673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91921079-T-C

81343673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91921079-T-G

81343674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91921078-G-C

81343674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91921078-G-T

http://identifiers.org/hco/5/GRCh38#81343686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91921066-C-A

81343686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91921066-C-G

81343686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91921066-C-T

81343693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91921061-G-T

81343719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91921035-A-G

http://identifiers.org/hco/5/GRCh38#81343734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91921020-A-C

81343734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91921020-A-G

81343744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91921010-A-G

81343756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91920998-G-A

81343756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91920998-G-T

81343861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91920897-T-C

81343900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91920861-G-C

81343938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91920824-A-G

81343946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91920821-C-T

81343973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91920794-G-T

81343989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91920768-G-A

81343989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91920768-G-C

81343989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91920768-G-T

http://identifiers.org/hco/5/GRCh38#81344005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91920752-C-A

81344005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91920752-C-T

http://identifiers.org/hco/5/GRCh38#81344087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91920674-C-A

81344101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91920655-T-C

81344143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91920614-C-T

81344203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91920554-G-A

81344203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91920554-G-T

81344211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense variant
orthologous variants: 91920546-T-C

81344314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91920461-G-A

81344314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91920461-G-T

81344430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91920392-T-C

81344612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91920241-G-T

81344874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91920008-G-A

81344874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91920008-G-C

81344874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91920008-G-T

81344964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense variant
orthologous variants: 91919918-G-A

81345036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense variant
orthologous variants: 91919846-T-G

81345064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91919821-G-T

81345107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91919798-C-T

http://identifiers.org/hco/5/GRCh38#81345118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91919789-C-A

http://identifiers.org/hco/5/GRCh38#81345144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91919778-A-C

81345182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91919751-T-C

81346110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91918845-A-G

81346128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91918817-G-A

81346128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91918817-G-T

81347703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91918421-T-C

81347852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91918284-G-A

81347852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91918284-G-T

81347867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 91918269-T-A

81347933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 91918203-G-A

81347933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 91918203-G-C

81347967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91918176-G-A

81347998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91918147-T-C

81348026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91918117-A-G

81348026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91918117-A-T

81349241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91917493-A-T

81349331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91917401-C-G

http://identifiers.org/hco/5/GRCh38#81349355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91917377-C-A

81349528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91917190-C-T

81350236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91916192-G-A

81350268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91916154-T-C

81350361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91916060-T-G

81350571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91915568-T-C

81350706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91915433-T-C

81350742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91915398-T-A

81350774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91915371-T-C

81350798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91915342-G-A

81350825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91915315-G-T

81350852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91915293-G-C

http://identifiers.org/hco/5/GRCh38#81351198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91914954-A-C

81351198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91914954-A-G

81353054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91914200-T-C

81353055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91914199-G-A

81353388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91913886-G-A

81353553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, undefined
orthologous variants: 91913712-A-T

81353657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91913624-A-G

81353689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91913610-C-T

81353740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91913563-C-T

81353902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91913396-T-A

http://identifiers.org/hco/5/GRCh38#81353941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91913359-A-C

http://identifiers.org/hco/5/GRCh38#81353988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91913314-C-A

81357327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91912905-A-G

81357380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91912860-G-A

81357532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91912719-T-G

81357635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91912604-T-A

81357635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91912604-T-C

81358323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91912130-C-T

81358342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91912111-A-G

81358520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 91911761-C-T

http://identifiers.org/hco/5/GRCh38#81359877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91911199-A-C

81359877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 91911199-A-G

81360149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91910915-G-C

81360165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91910899-T-C

81361587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91910172-C-T

81361666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91910091-G-T

81361675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91910083-T-C

81361686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91910072-C-T

81361940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91909896-T-C

81362060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91909777-A-G

81362133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91909742-G-C

81362155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91909720-A-T

81362837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91909159-A-T

81362903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91909094-A-G

81363143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91908764-C-T

81363247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91908698-C-T

http://identifiers.org/hco/5/GRCh38#81363296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91908643-A-C

81363715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91908251-T-C

81363719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91908247-A-G

81363719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91908247-A-T

http://identifiers.org/hco/5/GRCh38#81363724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91908244-C-A

http://identifiers.org/hco/5/GRCh38#81363774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91908194-C-A

81363774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91908194-C-T

81363819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, missense_variant
orthologous variants: 91908149-G-A

81363894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 91908074-A-G

81364039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91907945-A-G

81364039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91907945-A-T

81364190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91907797-T-C

81364292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91907747-T-A

81364302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91907737-T-C

81364671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91907383-C-T

81364740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91907332-A-T

81365398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91906752-T-C

81365436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91906710-T-A

81365636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91906527-T-C

81365862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91906353-G-A

81365949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91906259-C-T

81371628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91905822-G-C

81371628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91905822-G-T

81371655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, undefined
orthologous variants: 91905794-A-G

81371716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91905735-C-T

81371766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense variant
orthologous variants: 91905684-A-G

http://identifiers.org/hco/5/GRCh38#81371841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#91905609-A-C

81371891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91905564-T-G

81372072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91905383-A-G

81372111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91905347-C-T

81372620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91904921-C-T

81372843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91904743-A-G

81372859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91904727-G-A

81379598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91904469-A-T

81379621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91904446-G-A

http://identifiers.org/hco/5/GRCh38#81380221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91903990-A-C

81385482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91898614-A-G

81385482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91898614-A-T

81385575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91898536-G-C

81385655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91898469-A-G

http://identifiers.org/hco/5/GRCh38#81385683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91898446-C-A

http://identifiers.org/hco/5/GRCh38#81385714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91898415-C-A

81385714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91898415-C-T

http://identifiers.org/hco/5/GRCh38#81385899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91898220-A-C

81385941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91898177-T-A

http://identifiers.org/hco/5/GRCh38#81385946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91898172-C-A

81386009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91898111-A-G

http://identifiers.org/hco/5/GRCh38#81386035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91898085-C-A

81386035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91898085-C-G

81386035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91898085-C-T

http://identifiers.org/hco/5/GRCh38#81386530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91897628-A-C

81386649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91897142-T-C

81386710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91897079-T-A

81386733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91897056-T-G

81386882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91896920-G-A

81388067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91895785-G-A

81388150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91895707-T-A

81388235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91895627-G-C

81388306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91895565-A-G

81388597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91895040-G-A

81391082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91893701-C-T

81391084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91893699-A-T

81391158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91893615-T-A

81391404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91893318-A-G

81391834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91892639-T-C

81391886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91892590-C-G

81391886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91892590-C-T

81392006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91892471-G-A

http://identifiers.org/hco/5/GRCh38#81393926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91889828-C-A

81393926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron variant
orthologous variants: 91889828-C-T

81393943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, undefined
orthologous variants: 91889812-G-A

81393943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, undefined
orthologous variants: 91889812-G-C

81393943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, undefined
orthologous variants: 91889812-G-T

81393969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: intron_variant, undefined
orthologous variants: 91889791-A-G

http://identifiers.org/hco/5/GRCh38#81393987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: splice_donor_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#91889778-C-A

81393987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: splice_donor_variant, undefined
orthologous variants: 91889778-C-G

81393987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: splice_donor_variant, undefined
orthologous variants: 91889778-C-T

81394041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense_variant, undefined
orthologous variants: 91889724-T-A

81394041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense_variant, undefined
orthologous variants: 91889724-T-C

81394041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense_variant, undefined
orthologous variants: 91889724-T-G

81394092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense variant
orthologous variants: 91889673-T-C

http://identifiers.org/hco/5/GRCh38#81394095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#91889670-C-A

81394095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense variant
orthologous variants: 91889670-C-G

81394095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: missense variant
orthologous variants: 91889670-C-T

81394149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 91889618-A-G

81394149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24436
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 91889618-A-T