http://identifiers.org/hco/2/GRCh38#233354512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#87781016-C-A

233354512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 87781016-C-G

233354512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 87781016-C-T

http://identifiers.org/hco/2/GRCh38#233354554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87781058-C-A

233354554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: synonymous variant
orthologous variants: 87781058-C-T

http://identifiers.org/hco/2/GRCh38#233354599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87781103-C-A

233354599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: missense variant
orthologous variants: 87781103-C-G

233354599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: synonymous variant
orthologous variants: 87781103-C-T

233354611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: synonymous variant
orthologous variants: 87781115-G-A

233354611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: synonymous variant
orthologous variants: 87781115-G-T

http://identifiers.org/hco/2/GRCh38#233354907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87781345-C-A

233355109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87781509-G-T

233355130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87781534-C-G

233355130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87781534-C-T

233355141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87781546-C-T

233355151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87781556-C-T

233355241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87781619-G-T

233355280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87781702-A-G

233355290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87781714-C-T

233355502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87781938-C-T

233356534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87782313-G-A

233356805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87782587-G-T

233356899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87782677-G-T

233356960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87782709-G-A

233357050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, undefined
orthologous variants: 87782796-A-G

233357947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87783372-C-G

233373764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87800746-G-C

233373869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87800849-A-G

233373877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87800857-G-A

233373899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87800874-A-G

http://identifiers.org/hco/2/GRCh38#233380570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87803988-C-A

233380570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87803988-C-G

233381151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87804447-C-T

http://identifiers.org/hco/2/GRCh38#233385803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87805721-C-A

233385803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87805721-C-T

233386027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87805950-G-A

233386027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87805950-G-C

http://identifiers.org/hco/2/GRCh38#233386552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87806385-A-C

233386552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87806385-A-G

233386552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87806385-A-T

233386923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87806635-G-C

http://identifiers.org/hco/2/GRCh38#233388007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#87807850-C-A

233388007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87807850-C-T

http://identifiers.org/hco/2/GRCh38#233388046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#87807872-C-A

233388046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87807872-C-T

http://identifiers.org/hco/2/GRCh38#233388568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87808482-C-A

233388568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87808482-C-T

233389205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87808637-T-C

http://identifiers.org/hco/2/GRCh38#233389494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87808861-C-A

http://identifiers.org/hco/2/GRCh38#233389559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87808925-C-A

233389760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87809063-C-T

233390058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87809308-C-T

233390194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87809380-C-T

233391202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87810347-A-G

233391202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87810347-A-T

233391236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87810381-G-T

http://identifiers.org/hco/2/GRCh38#233391262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87810430-C-A

http://identifiers.org/hco/2/GRCh38#233391298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87810443-A-C

233391529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87810634-C-T

233392051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87811175-G-T

http://identifiers.org/hco/2/GRCh38#233392132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87811245-C-A

233392133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, missense_variant
orthologous variants: 87811246-T-C

http://identifiers.org/hco/2/GRCh38#233392149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87811262-C-A

233392149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, missense_variant
orthologous variants: 87811262-C-T

233404414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87814764-C-T

233406277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87815325-A-G

233407112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87817660-A-G

233407195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87817743-T-C

233407259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87817808-C-T

233407829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron variant
orthologous variants: 87818788-A-G

233408442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87819074-A-G

233408456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87819088-T-C

233408555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87819153-G-C

233408808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87819473-G-A

233408808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 87819473-G-T

233409089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87819704-A-G

233409115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87819726-A-G

233409128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87819739-G-T

233409458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87820017-A-G

233409508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87820060-T-G

233409776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87820255-C-T

http://identifiers.org/hco/2/GRCh38#233409864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87820311-A-C

233409874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87820319-C-G

233409874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87820319-C-T

233410331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87820615-C-T

233410332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87820616-G-A

http://identifiers.org/hco/2/GRCh38#233410894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87821177-C-A

233411511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87821770-A-G

233411609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87821844-T-G

233411642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87821876-A-G

233411706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87821927-A-G

233411743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87821967-C-T

233411748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87821972-C-T

233411815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87822037-C-T

233411857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87822068-G-A

233411857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87822068-G-T

233413270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87823027-C-G

233413270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87823027-C-T

233413455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87823330-G-A

233413455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87823330-G-T

233413472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87823347-C-T

233413649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87823482-C-T

233414579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87824504-A-G

233414833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87824734-G-A

233415143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87824904-C-T

233419003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87828773-T-A

233419351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 87829104-T-C

http://identifiers.org/hco/2/GRCh38#233419454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87829178-C-A

233419787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87829461-G-A

233419898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87829601-A-G

233419900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87829603-G-A

233419900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87829603-G-T

233420240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87830060-G-A

233420544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87830317-T-C

233421333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87831234-C-G

233421614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87833872-T-C

233421756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87834008-C-T

233421864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87834087-C-G

233422024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87834244-C-T

233422261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87834375-A-G

233423128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87835265-T-C

233423305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87835418-C-T

233428372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87839498-T-C

233428470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87839577-G-C

233428843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87839880-C-T

233429161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87840099-G-A

233429250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87840198-T-C

233429515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87840425-A-G

233430431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87841247-C-T

233430458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87841274-A-G

233430557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87841414-C-G

233434153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87842273-G-A

233434172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87842289-C-T

233435121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87843541-G-A

233435190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87843590-G-A

233435243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87843624-A-G

http://identifiers.org/hco/2/GRCh38#233435760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87844034-C-A

233435760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87844034-C-G

233435994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87844241-T-A

http://identifiers.org/hco/2/GRCh38#233436021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87844264-C-A

233436021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87844264-C-G

233436037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87844279-A-G

http://identifiers.org/hco/2/GRCh38#233436165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87844376-C-A

233436165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87844376-C-T

http://identifiers.org/hco/2/GRCh38#233436220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87844431-A-C

233436521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87844716-G-A

233436521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87844716-G-T

233436554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87844746-G-A

http://identifiers.org/hco/2/GRCh38#233436704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87844863-C-A

http://identifiers.org/hco/2/GRCh38#233437274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87845513-C-A

233437274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87845513-C-T

233437516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87845738-C-T

http://identifiers.org/hco/2/GRCh38#233437517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87845739-C-A

233437517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87845739-C-T

233437574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87845787-G-C

233437574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87845787-G-T

233437744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87845900-C-T

233437820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87845958-T-C

233437992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87846126-G-T

http://identifiers.org/hco/2/GRCh38#233438071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87846171-C-A

233438071-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87846171-C-G

233438077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87846177-A-T

233438102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87846189-G-T

233438114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87846198-G-C

233438114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87846198-G-T

http://identifiers.org/hco/2/GRCh38#233438145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87846222-C-A

233438145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87846222-C-T

233438146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87846223-T-C

233438175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87846247-T-G

233438189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 87846253-A-G

233438257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87846321-A-G

233438257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87846321-A-T

233438392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87846456-T-A

233439541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87847989-G-T

233441666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87849069-G-T

233441751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87849169-A-G

233442332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87849593-G-A

233442332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87849593-G-T

233443608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87850457-G-A

233443659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87850508-A-G

233443817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 87850663-C-G

http://identifiers.org/hco/2/GRCh38#233443872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#87850715-C-A

233444255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87851045-C-T

233444276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87851065-T-G

233444354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87851154-C-T

233445541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87851712-G-A

233445541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87851712-G-T

http://identifiers.org/hco/2/GRCh38#233445552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87851723-A-C

233445552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87851723-A-T

233445676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87851847-G-A

233445676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87851847-G-C

233446799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87852296-A-G

233446833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87852381-C-T

http://identifiers.org/hco/2/GRCh38#233446923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87852450-C-A

233446942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87852469-A-G

233446942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87852469-A-T

233447096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87852578-G-A

http://identifiers.org/hco/2/GRCh38#233447188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87852622-C-A

233447188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87852622-C-T

233447228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87852654-C-T

http://identifiers.org/hco/2/GRCh38#233447345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87852761-C-A

233447345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87852761-C-T

http://identifiers.org/hco/2/GRCh38#233447428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87852854-C-A

233447428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87852854-C-T

233447486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87852901-T-C

233447594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87853006-T-C

233447594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87853006-T-G

233447699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87853084-A-G

233447774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87853139-G-A

233447774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87853139-G-C

233447774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87853139-G-T

233447778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87853143-T-C

233447808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87853173-C-T

http://identifiers.org/hco/2/GRCh38#233448047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87853377-C-A

233448047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 87853377-C-T

233448082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87853411-T-C

233448082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 87853411-T-G

233448119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87853448-T-G

233448149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87853478-G-A

233448149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87853478-G-C

233448211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87853548-T-C

233448419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87853737-G-A

233449240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 87853910-C-T

233449383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 87854053-G-T

233449530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87854159-T-A

233449732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87854358-C-G

233449868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87854506-G-T

233449871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87854509-T-G

233449909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87854524-G-A

233449909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87854524-G-T

http://identifiers.org/hco/2/GRCh38#233449923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87854529-C-A

233449986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87854592-C-G

233449986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87854592-C-T

233450043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87854649-G-A

233450043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87854649-G-C

233450090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87854705-G-A

233450309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87854880-T-C

233450649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87855148-C-T

233450690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87855184-C-T

233450796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87855278-G-A

233450796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87855278-G-T

233450805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87855292-T-A

233450805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87855292-T-C

233451008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87855490-C-T

233451876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87857385-T-C

http://identifiers.org/hco/2/GRCh38#233451899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87857407-C-A

233451899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87857407-C-T

233451902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87857410-G-A

233451904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87857412-G-A

233452040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87857539-C-T

233453403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87858505-C-T

http://identifiers.org/hco/2/GRCh38#233453629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87858725-C-A

233454541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87859349-T-C

233454599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87859394-T-A

233454599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87859394-T-G

233454618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87859419-G-A

233454618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87859419-G-C

http://identifiers.org/hco/2/GRCh38#233454657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87859511-A-C

233454692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87859563-G-A

233454692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87859563-G-T

233456781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87860942-A-G

233456823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87861762-G-A

233456823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87861762-G-C

233456823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87861762-G-T

233457017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87861943-A-G

http://identifiers.org/hco/2/GRCh38#233457030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87861956-C-A

http://identifiers.org/hco/2/GRCh38#233457052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87861978-C-A

233457071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87861999-G-A

233457071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87861999-G-C

http://identifiers.org/hco/2/GRCh38#233457083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87862003-C-A

233457083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87862003-C-T

233457184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87862079-T-C

233457586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87862383-A-G

233457642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 87862432-A-G

233457822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87862600-G-A

233457822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87862600-G-C

233457950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87862714-G-A

233457950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87862714-G-C

233457950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87862714-G-T

233457987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87862758-G-A

233458131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87862899-G-A

233458131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87862899-G-T

233458234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87863014-G-A

233458234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87863014-G-C

233458234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87863014-G-T

http://identifiers.org/hco/2/GRCh38#233458304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87863080-C-A

233458304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87863080-C-T

233458415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87863192-G-A

233458415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87863192-G-T

233459289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87863636-C-T

233459382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87863708-C-T

233459726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87863978-A-G

233461647-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87865285-C-G

233461784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87865405-T-C

233462085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87865649-C-T

http://identifiers.org/hco/2/GRCh38#233462229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87865797-C-A

233462229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87865797-C-T

233462259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87865817-G-A

233462259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87865817-G-T

233462344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 87865872-C-G

233462344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 87865872-C-T

233462373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87865901-C-T

http://identifiers.org/hco/2/GRCh38#233462660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87866085-C-A

233462660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 87866085-C-G

233462660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 87866085-C-T

233462762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87866183-G-A

233462762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87866183-G-T

http://identifiers.org/hco/2/GRCh38#233462770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87866191-C-A

233462770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87866191-C-T

233462793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87866209-G-A

233462793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87866209-G-T

233462814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87866231-G-T

233462832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87866249-A-T

http://identifiers.org/hco/2/GRCh38#233463895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87866668-C-A

233463895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 87866668-C-G

233463895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87866668-C-T

233464247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87867001-G-A

233464247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 87867001-G-T

233464335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87867081-C-G

233464678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87867329-C-T

233464744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87867371-C-T

233464751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87867378-G-A

233464751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87867378-G-C

233464827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87867433-C-T

233464828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87867434-G-A

233464979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 87867600-T-C

233468251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87869001-G-A

233468364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87869032-G-A

233468364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87869032-G-T

233468629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87869294-G-A

233468629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87869294-G-T

233469055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87869797-A-G

233469055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 87869797-A-T

http://identifiers.org/hco/2/GRCh38#233469898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87870612-C-A

233469898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87870612-C-T

http://identifiers.org/hco/2/GRCh38#233470259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87870980-C-A

233470259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87870980-C-T

http://identifiers.org/hco/2/GRCh38#233470323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87871014-C-A

233470323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87871014-C-G

233470323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87871014-C-T

233470417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87871061-T-C

233470509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87871127-A-G

http://identifiers.org/hco/2/GRCh38#233470545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87871150-C-A

233470661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87871234-T-C

233470997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87871425-G-A

233470997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87871425-G-T

http://identifiers.org/hco/2/GRCh38#233471087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87871474-C-A

233471087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87871474-C-T

233471159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87871539-A-G

233471341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87871717-A-G

233471793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87871942-G-A

233471793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87871942-G-C

233471793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87871942-G-T

http://identifiers.org/hco/2/GRCh38#233471960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#87872079-C-A

233471960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2851
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 87872079-C-T