http://identifiers.org/hco/1/GRCh38#206635577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#131065992-C-A

206635577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131065992-C-T

206635654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 131065934-A-G

http://identifiers.org/hco/1/GRCh38#206635679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#131065912-C-A

206635679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 131065912-C-T

206635722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 131065873-G-A

206635722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 131065873-G-T

206635748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131065847-G-A

206635748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 131065847-G-T

http://identifiers.org/hco/1/GRCh38#206635931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#131065767-C-A

206635931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131065767-C-T

206636006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131065726-G-A

206636006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131065726-G-C

206636006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131065726-G-T

http://identifiers.org/hco/1/GRCh38#206636165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131065645-A-C

http://identifiers.org/hco/1/GRCh38#206636170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131065638-C-A

206636170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131065638-C-T

http://identifiers.org/hco/1/GRCh38#206636191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#131065617-C-A

206636191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131065617-C-T

http://identifiers.org/hco/1/GRCh38#206636848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131065105-C-A

206636848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131065105-C-T

http://identifiers.org/hco/1/GRCh38#206637544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131064189-C-A

206637711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131064045-T-A

206637711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131064045-T-G

206637718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131064038-T-C

206637718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131064038-T-G

206637721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131064035-T-C

206637721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 131064035-T-G

206637815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131063951-G-A

206637815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131063951-G-T

http://identifiers.org/hco/1/GRCh38#206637903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131063646-C-A

206637903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131063646-C-T

206638107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131063445-A-G

206638107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131063445-A-T

206638134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131063424-T-C

206638194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131063380-A-G

206638269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131063312-G-T

http://identifiers.org/hco/1/GRCh38#206638315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131063294-C-A

206638315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131063294-C-T

http://identifiers.org/hco/1/GRCh38#206638423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131063251-C-A

206638423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131063251-C-T

206638496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131063195-G-T

206638529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131063177-T-A

206638529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131063177-T-C

206638714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131063037-T-C

206638983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131062851-A-G

206639245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131062728-C-G

206639245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131062728-C-T

206639269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131062706-G-A

206639882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131062461-T-C

http://identifiers.org/hco/1/GRCh38#206639923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131062420-C-A

206639923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131062420-C-T

206639955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131062368-G-A

206639955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131062368-G-C

206639955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131062368-G-T

206639978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131062345-A-G

206640073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131062262-T-C

206643007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131060820-T-A

206643123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131060701-A-G

206643184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131060644-A-G

http://identifiers.org/hco/1/GRCh38#206643235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131060597-A-C

206643296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131060536-T-G

206643298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131060534-C-T

http://identifiers.org/hco/1/GRCh38#206643424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131060408-A-C

206643424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131060408-A-G

206643578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131060285-A-G

206643654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131060209-G-T

206643678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131060184-G-A

206643732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131060138-G-A

206644443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131059681-T-C

206644767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131059452-T-C

206644816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131059399-A-G

206644830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131059385-A-G

206644833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131059383-G-T

206647061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131058660-G-A

206647348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131058026-T-G

http://identifiers.org/hco/1/GRCh38#206647368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131058001-A-C

206647368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131058001-A-T

206647391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131057977-A-T

206647457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 131057911-C-T

206647793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131057578-C-T

206647808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131057563-C-T

206647829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131057542-G-A

206647829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131057542-G-C

206647946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131057425-G-A

206647946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131057425-G-C

http://identifiers.org/hco/1/GRCh38#206648234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131057137-C-A

206648234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131057137-C-T

206648258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131057113-A-G

206648606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131056765-C-T

206648627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131056744-C-T

206648661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131056710-A-G

206648668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 131056703-T-C

206648922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131056452-G-A

206648922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 131056452-G-C

206648991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131056386-A-G

206648998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131056378-T-C

http://identifiers.org/hco/1/GRCh38#206649086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131056282-A-C

206649107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131056261-T-C

http://identifiers.org/hco/1/GRCh38#206649136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131056233-C-A

206649136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131056233-C-T

http://identifiers.org/hco/1/GRCh38#206649197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131056171-A-C

206649200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131056168-T-C

206649210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131056158-T-G

206649219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131056149-G-A

206649219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131056149-G-T

206649233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131056135-G-A

206649241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131056129-C-T

http://identifiers.org/hco/1/GRCh38#206649302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131055892-C-A

206649302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131055892-C-T

206649339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131055827-G-A

206649339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131055827-G-T

206649915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131054994-C-T

206652253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131054145-T-C

206652301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131054097-A-G

206652413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131053996-T-C

206652433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131053978-A-G

206652487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131053925-C-T

206653516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131053435-C-T

206653635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131053340-T-G

206654189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131052821-A-G

206654189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131052821-A-T

206654381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131052637-C-T

206654551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131052479-A-G

http://identifiers.org/hco/1/GRCh38#206654664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131052374-C-A

206654927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131051895-A-G

http://identifiers.org/hco/1/GRCh38#206654998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131051838-A-C

206655027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 131051809-A-G

206657022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131050857-A-G

206657125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131050760-G-C

206658524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131050021-T-C

206658612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131049963-C-T

206658722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131049877-C-T

206658724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131049875-G-A

http://identifiers.org/hco/1/GRCh38#206658786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131049823-C-A

206659169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131048921-C-G

206659221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131048871-A-G

206659276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131048817-G-T

206659612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131048535-A-T

206659649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131048520-T-C

http://identifiers.org/hco/1/GRCh38#206659820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131048403-A-C

206659820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131048403-A-G

http://identifiers.org/hco/1/GRCh38#206659825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131048398-C-A

206659828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131048395-A-G

206659883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131048354-C-G

http://identifiers.org/hco/1/GRCh38#206660094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131048185-A-C

206660351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131047944-G-C

206660420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131047874-A-G

206660933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131047428-G-A

206662875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131046456-G-A

206662932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131046422-G-A

206663287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131045875-C-G

206663287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131045875-C-T

http://identifiers.org/hco/1/GRCh38#206663315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131045833-A-C

206663474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131044925-T-C

206663683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131044723-C-G

206663767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131044639-G-T

http://identifiers.org/hco/1/GRCh38#206663997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131044465-A-C

206664394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131043849-G-A

206664449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 131043786-A-G

206664796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131043412-G-A

http://identifiers.org/hco/1/GRCh38#206664904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131043315-A-C

206665096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131043135-C-G

206665130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131043101-A-G

http://identifiers.org/hco/1/GRCh38#206665412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131042307-C-A

206665462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131042269-C-T

206665652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131042125-A-T

206665957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131041857-G-A

206671556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131039698-T-C

206671897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131039324-G-A

206671990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131039243-G-A

206671990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131039243-G-T

206672055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131039173-T-C

206672146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131039065-C-T

206672400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131038869-C-T

206672468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131038811-A-T

206672523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131038752-C-T

206672677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131038635-T-C

206673407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131038022-C-T

206673475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131037965-G-A

206673483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131037957-T-C

206675124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131035788-C-T

206675292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131035644-C-T

http://identifiers.org/hco/1/GRCh38#206675452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131035481-C-A

http://identifiers.org/hco/1/GRCh38#206675505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131035437-C-A

206675533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131035398-C-T

http://identifiers.org/hco/1/GRCh38#206678273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131033887-A-C

206678351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131033779-A-G

206678554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131033577-T-G

206678645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131033512-A-G

206678662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131033495-C-T

206679220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131031970-G-A

206679974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131031588-G-A

206680091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131031502-A-G

http://identifiers.org/hco/1/GRCh38#206680251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131031342-C-A

206680261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131031332-C-G

206680264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131031329-A-T

206680349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131031279-G-A

206680384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131031242-G-A

206680477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131031165-C-T

206680535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131031107-A-G

206681018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131030015-T-C

206681499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131029576-C-T

206681572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131029494-T-C

206681706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131029248-T-C

206682100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 131028899-A-G

206682342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131028617-C-T

206682805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131028168-G-A

http://identifiers.org/hco/1/GRCh38#206683102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131027196-C-A

206683102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131027196-C-T

206683291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131027060-G-A

206683341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131027029-G-T

206683382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026994-G-A

206683382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026994-G-T

http://identifiers.org/hco/1/GRCh38#206683383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131026993-C-A

206683383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026993-C-T

206683394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026984-A-G

http://identifiers.org/hco/1/GRCh38#206683410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131026968-C-A

206683410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026968-C-T

206683427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026951-A-G

206683477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026899-C-T

206683497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026887-C-T

206683498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026886-G-A

206683498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026886-G-C

206683498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026886-G-T

206683536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026859-A-G

206683624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131026790-G-T

206683690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131026739-T-C

206683710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131026721-G-A

206683710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 131026721-G-C

206683747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026691-T-C

http://identifiers.org/hco/1/GRCh38#206683752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131026686-C-A

206683752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026686-C-T

206683780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026658-C-G

206683799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026638-G-A

206683821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026616-T-A

206683897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026540-T-C

206684068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026433-T-C

206684082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026405-T-C

206684097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026397-A-G

206684115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026379-A-G

http://identifiers.org/hco/1/GRCh38#206684154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131026342-C-A

206684154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026342-C-T

http://identifiers.org/hco/1/GRCh38#206684216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#131026263-A-C

206684239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026220-C-T

206684240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026219-A-G

206684250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026211-G-A

206684335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3094
most severe consequence: non coding transcript exon variant
orthologous variants: 131026139-G-T