237813557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91077771-G-T

237813558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91077772-T-C

237813587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 91077800-T-C

http://identifiers.org/hco/2/GRCh38#237813588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91077801-C-A

237813588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 91077801-C-G

237813645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91077858-T-A

237813658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91077871-A-G

237813760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91077952-A-G

237814955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91078067-G-A

237814957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91078069-A-G

237815045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91078148-C-T

237815058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91078161-A-G

237815071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91078174-T-C

237815235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91078399-A-G

237815350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91078503-C-G

237815366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91078518-C-G

237815428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91078582-T-A

237815583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91078700-G-T

237815997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91078956-A-G

237815997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91078956-A-T

237816030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91078990-G-A

237816236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91079136-C-G

237816316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91079211-T-C

237816319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91079214-G-A

237816466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91079361-C-G

237816466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91079361-C-T

237816537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91079432-G-A

237816672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91079554-A-G

237816753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91079637-C-T

237816881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91079775-G-A

237816881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91079775-G-T

237816939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91079831-A-G

237816939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91079831-A-T

http://identifiers.org/hco/2/GRCh38#237817036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91079927-C-A

237817036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 91079927-C-T

237817048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91079939-T-A

237817061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91079952-A-G

237817080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 91079971-G-A

237817128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91080019-A-G

237817148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91080039-T-G

237817159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 91080050-T-C

237817191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91080082-G-A

237817208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91080099-A-G

237817309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 91080200-T-C

237817341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91080232-A-T

237817425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91080310-G-C

237817695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91080553-T-C

237817695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91080553-T-G

237817763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 91080621-A-T

237817877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91080702-A-G

237818030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91080855-C-T

http://identifiers.org/hco/2/GRCh38#237818063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91080888-A-C

237818063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91080888-A-T

237818070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91080895-T-A

237818177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91080996-G-A

237818177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91080996-G-C

237818300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91081116-A-G

http://identifiers.org/hco/2/GRCh38#237818308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91081124-A-C

http://identifiers.org/hco/2/GRCh38#237818370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91081156-C-A

237818409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 91081195-C-T

http://identifiers.org/hco/2/GRCh38#237818434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91081220-A-C

237818434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 91081220-A-G

237818440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 91081226-T-C

237818494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 91081277-A-G

237818494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 91081277-A-T

237818509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 91081292-T-C

http://identifiers.org/hco/2/GRCh38#237818552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91081338-C-A

237818552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91081338-C-T

237818636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91081416-A-G

237818701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91081465-G-T

237818859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91081563-A-G

237818931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91081646-A-G

http://identifiers.org/hco/2/GRCh38#237818952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91081667-C-A

237818952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 91081667-C-T

237818993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91081708-G-A

237818993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91081708-G-T

237819044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91081760-A-G

237819091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91081800-G-A

http://identifiers.org/hco/2/GRCh38#237819349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#91082020-C-A

237819349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91082020-C-G

http://identifiers.org/hco/2/GRCh38#237819410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#91082068-C-A

237819410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91082068-C-G

237819413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 91082071-G-A

237819665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91082479-T-C

237819707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91082538-C-G

237819714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91082545-A-G

237819873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91082727-C-T

237820187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91083119-T-C

http://identifiers.org/hco/2/GRCh38#237820227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91083153-C-A

237820227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 91083153-C-T

237820248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91083174-A-G

237820250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91083176-A-G

237820429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91083338-T-A

237820430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91083339-T-C

http://identifiers.org/hco/2/GRCh38#237820495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91083399-A-C

237820495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91083399-A-G

237820495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 91083399-A-T

http://identifiers.org/hco/2/GRCh38#237820989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91084296-C-A

237821326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91084626-T-C

237821357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91084651-A-G

237821388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91084681-G-T

237821790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91084833-T-G

237821809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91084852-A-G

237821809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91084852-A-T

http://identifiers.org/hco/2/GRCh38#237821947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91085471-C-A

237821947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91085471-C-T

237821986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91085518-T-C

237822007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91085539-A-G

237822168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91088296-A-G

237822903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91089513-C-T

http://identifiers.org/hco/2/GRCh38#237822904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91089514-A-C

237823348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91089989-G-A

237823348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91089989-G-T

237823427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91090065-T-A

237823427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91090065-T-C

237823470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91090110-A-G

237823470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91090110-A-T

237823477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91090117-A-G

237823477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91090117-A-T

237823482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91090122-T-A

237823482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91090122-T-C

237823494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91090134-G-A

237823494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91090134-G-T

http://identifiers.org/hco/2/GRCh38#237823504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91090144-A-C

237823504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91090144-A-G

237823525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91090165-A-G

http://identifiers.org/hco/2/GRCh38#237823533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91090173-C-A

237823533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 91090173-C-T

237823564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91090204-A-G

237823570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91090210-T-C

http://identifiers.org/hco/2/GRCh38#237823576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91090216-C-A

237823576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91090216-C-T

237823857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91090403-G-T

237824017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91090534-G-A

237824019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91090536-G-A

http://identifiers.org/hco/2/GRCh38#237824088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91090602-A-C

http://identifiers.org/hco/2/GRCh38#237824145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91090649-C-A

237824145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91090649-C-T

http://identifiers.org/hco/2/GRCh38#237824159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91090662-A-C

237824220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91090707-G-A

237824220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91090707-G-T

237824256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 91090740-G-A

237824269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 91090753-C-T

237824278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 91090762-T-G

237824368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91090851-A-T

http://identifiers.org/hco/2/GRCh38#237824376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91090859-A-C

http://identifiers.org/hco/2/GRCh38#237824390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91090873-A-C

237824408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91090891-A-G

http://identifiers.org/hco/2/GRCh38#237824476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91090955-C-A

237824476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91090955-C-T

http://identifiers.org/hco/2/GRCh38#237824487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91090965-C-A

237824487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91090965-C-T

237824562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91091055-G-A

237825917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91091347-G-T

237826015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91091445-A-G

237826189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91091545-A-G

237826374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91091698-T-G

237826538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91091842-A-G

237826986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91092263-G-A

237827187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91092595-A-T

237827265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91092651-A-G

237827277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91092663-G-T

237827298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91092684-A-G

237827323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91092709-A-G

237827353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91092740-G-A

237827353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91092740-G-T

237827358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91092745-A-G

237827535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91092919-A-G

237827538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91092922-A-G

237827549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91092933-G-A

237827735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91093108-G-A

237827804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91093177-A-G

237828333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91093743-A-G

237828656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91093890-G-C

http://identifiers.org/hco/2/GRCh38#237828915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91094137-C-A

http://identifiers.org/hco/2/GRCh38#237829118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91094435-C-A

237829118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91094435-C-T

237829194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91094498-G-T

237829310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91094614-G-A

237829312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 91094616-G-A

237829317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91094621-G-A

237829363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91094667-G-A

237829363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91094667-G-T

237829364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91094668-G-C

237829429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91094733-T-C

237832548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91096235-G-A

237832655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91096333-T-C

237832689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91096365-C-T

237832706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91096382-T-C

237832717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91096392-C-T

237832721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91096396-A-G

http://identifiers.org/hco/2/GRCh38#237834043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91096461-C-A

237834043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91096461-C-G

http://identifiers.org/hco/2/GRCh38#237834066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91096484-C-A

237834066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91096484-C-T

http://identifiers.org/hco/2/GRCh38#237834123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91096541-C-A

237834123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91096541-C-G

237834123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91096541-C-T

237834128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 91096546-T-A

237834128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91096546-T-C

237834161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91096579-T-C

http://identifiers.org/hco/2/GRCh38#237834233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91096634-C-A

http://identifiers.org/hco/2/GRCh38#237834234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91096635-C-A

237834257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91096658-G-C

237834257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 91096658-G-T

http://identifiers.org/hco/2/GRCh38#237834281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91096682-C-A

237834281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91096682-C-T

237834320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91096721-T-C

237834347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 91096748-T-C

http://identifiers.org/hco/2/GRCh38#237834536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91096914-C-A

http://identifiers.org/hco/2/GRCh38#237834559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91096937-C-A

http://identifiers.org/hco/2/GRCh38#237841930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#91097895-C-A

237842212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91098163-T-C

237842682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91098393-A-G

237842791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24756
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 91098502-G-T