http://identifiers.org/hco/18/GRCh38#23599071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12385559-A-C

23599564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3 prime UTR variant
orthologous variants: 12386035-G-A

23600059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12386517-A-G

23600136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12386588-A-T

23600356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12386790-T-C

23600392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12386824-T-C

23600393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12386825-A-G

23600401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12386833-A-G

23600579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12387012-A-G

23600615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12387044-A-G

23600680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12387109-C-T

http://identifiers.org/hco/18/GRCh38#23600740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12387169-C-A

23600773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12387283-T-G

23600821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12387332-G-A

http://identifiers.org/hco/18/GRCh38#23600822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12387333-C-A

23600822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12387333-C-T

http://identifiers.org/hco/18/GRCh38#23600957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12387454-C-A

23600961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12387458-G-T

23600994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12387489-T-A

23600994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12387489-T-C

23600994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12387489-T-G

23601060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 12387550-T-C

23601068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 12387558-G-A

23601068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 12387558-G-C

23601068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 12387558-G-T

23601156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 12387611-G-T

23601340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387789-T-A

23601340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387789-T-C

23601345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387794-A-G

23601377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387823-G-A

23601377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387823-G-T

http://identifiers.org/hco/18/GRCh38#23601400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12387847-C-A

23601400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387847-C-T

23601431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387876-C-T

http://identifiers.org/hco/18/GRCh38#23601433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12387878-C-A

23601433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387878-C-G

23601433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12387878-C-T

23609932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12391591-G-A

23611975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12393883-G-T

http://identifiers.org/hco/18/GRCh38#23612060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12393963-C-A

23612170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12394069-A-G

23612221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12394121-T-G

23612229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12394129-C-T

23612235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12394138-T-C

23612245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12394146-G-A

23612245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12394146-G-T

23612289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12394176-T-A

23612289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12394176-T-C

http://identifiers.org/hco/18/GRCh38#23612301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12394188-C-A

23612301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12394188-C-T

23612320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12394206-T-C

http://identifiers.org/hco/18/GRCh38#23612329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12394215-A-C

23612329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12394215-A-G

23617368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12394878-A-G

23617476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12394972-T-C

http://identifiers.org/hco/18/GRCh38#23617546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12395029-C-A

http://identifiers.org/hco/18/GRCh38#23617553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12395036-C-A

23617725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12395162-G-A

23617725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12395162-G-T

23617956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12395343-A-G

http://identifiers.org/hco/18/GRCh38#23618006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12395391-C-A

23618033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12395414-C-T

23618166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12395498-G-A

http://identifiers.org/hco/18/GRCh38#23618255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12395568-C-A

http://identifiers.org/hco/18/GRCh38#23619350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#12401388-A-C

http://identifiers.org/hco/18/GRCh38#23619415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12401448-C-A

23619415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12401448-C-T

23619427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12401460-T-C

http://identifiers.org/hco/18/GRCh38#23619485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#12401480-C-A

23619485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 12401480-C-T

23619494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 12401487-A-G

23619543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12401519-G-A

23619543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12401519-G-T

http://identifiers.org/hco/18/GRCh38#23619573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12401549-C-A

23619573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12401549-C-T

23619615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12401591-G-T

23619658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12401625-T-A

http://identifiers.org/hco/18/GRCh38#23619680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12401648-C-A

23619680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12401648-C-T

23619789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12401721-G-A

23621115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12402195-G-A

23621115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12402195-G-C

23621208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12402266-G-A

23621208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12402266-G-C

23621308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12402354-G-A

23621503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12402467-A-G

23622111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12402831-A-G

23622169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12402886-A-G

23622411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12403072-C-G

23624416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12404187-A-G

23624427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12404198-T-A

http://identifiers.org/hco/18/GRCh38#23624435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12404206-C-A

23624435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12404206-C-T

23625073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12404788-C-T

http://identifiers.org/hco/18/GRCh38#23625094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12404805-C-A

23625646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12404892-C-T

23625660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12404906-A-T

23625751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12405021-G-A

http://identifiers.org/hco/18/GRCh38#23625798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12405063-C-A

23625934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12405155-T-C

23625977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12405205-T-A

23625977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12405205-T-C

23626051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12405277-C-T

23626219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12405431-C-T

23626406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12406022-G-A

23626692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12406266-T-G

23626754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12406327-C-T

23626963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12406928-A-G

23626980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12406941-C-T

23627015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12406976-G-C

23627173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12407173-T-C

23627237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12407224-C-G

http://identifiers.org/hco/18/GRCh38#23628377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12407998-A-C

23628377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12407998-A-G

http://identifiers.org/hco/18/GRCh38#23628413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12408034-C-A

23628413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 12408034-C-T

23629540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12408510-T-C

23629554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12408524-A-G

http://identifiers.org/hco/18/GRCh38#23629810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#12408734-C-A

23629810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12408734-C-T

23629822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12408745-T-G

23631066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409701-T-A

23631665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409842-G-A

23631693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409869-A-G

23631748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409922-G-T

http://identifiers.org/hco/18/GRCh38#23631804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12409979-A-C

23631806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409981-G-A

23631812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12409987-C-T

23631870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410070-A-G

23631948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410144-A-G

23632116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12410305-A-T

23632770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 12411691-G-C

23633713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412509-G-A

23633951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412659-A-G

23633951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412659-A-T

23633957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412665-G-T

23634017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412727-G-T

23634043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12412739-G-A

23634190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412883-G-T

23634226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412914-T-A

23634226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412914-T-C

23634227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412915-A-G

23634243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412929-G-A

23634243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412929-G-C

23634243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12412929-G-T

23634745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413310-A-G

23634745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413310-A-T

23634967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413511-A-T

23635503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12413800-T-G

23635706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12414008-G-A

23635886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12414189-G-A

23635970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12414294-C-T

23638755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415231-G-A

23638755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415231-G-T

http://identifiers.org/hco/18/GRCh38#23638805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12415279-C-A

23638888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 12415399-A-T

23638959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415470-G-A

23638959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12415470-G-T

23640459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12417053-G-A

23643260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418358-G-A

23643260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418358-G-T

23643490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418568-C-T

23643848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12418883-T-C

23644030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419021-C-G

23644032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419023-G-A

23644032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419023-G-T

http://identifiers.org/hco/18/GRCh38#23644044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12419035-C-A

23644044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419035-C-G

23644044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419035-C-T

23644045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419036-A-G

http://identifiers.org/hco/18/GRCh38#23644204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12419182-A-C

23644308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419271-A-G

23644571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419547-A-G

23645235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419792-C-T

23645297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419848-T-A

23645297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419848-T-C

23645651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12419918-G-A

23645751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420014-G-A

http://identifiers.org/hco/18/GRCh38#23645886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12420131-A-C

23645886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420131-A-G

23645909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420150-T-C

23645955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12420193-T-C

23646064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12423649-C-G

http://identifiers.org/hco/18/GRCh38#23646116-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12423701-A-C

http://identifiers.org/hco/18/GRCh38#23646118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12423703-C-A

23646118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12423703-C-G

23646145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12423730-C-G

http://identifiers.org/hco/18/GRCh38#23646170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12423755-A-C

23646170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12423755-A-G

23646171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12423756-G-A

23646171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12423756-G-T

http://identifiers.org/hco/18/GRCh38#23646320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12423903-C-A

23646329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12423909-T-A

23646330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12423910-G-A

23646330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12423910-G-C

23646330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12423910-G-T

23646336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12423915-G-T

http://identifiers.org/hco/18/GRCh38#23646380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12423953-C-A

23646380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12423953-C-G

23646388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12423961-A-G

23646395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12423968-G-A

23646395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12423968-G-T

http://identifiers.org/hco/18/GRCh38#23646448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12424000-C-A

23646543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12424093-T-C

23646546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12424096-A-G

23646607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12424156-A-T

http://identifiers.org/hco/18/GRCh38#23646632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12424181-C-A

23646632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12424181-C-T

23646658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12424206-G-A

23646658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12424206-G-T

http://identifiers.org/hco/18/GRCh38#23646691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12424241-C-A

23647724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12427672-G-T

23647733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12427682-G-A

23647822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12427769-C-T

23647851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12427798-G-C

23647860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12427807-A-G

http://identifiers.org/hco/18/GRCh38#23647875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12427822-A-C

23647905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12427851-A-G

23647907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 12427853-T-C

http://identifiers.org/hco/18/GRCh38#23648052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12427950-C-A

23648052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12427950-C-T

http://identifiers.org/hco/18/GRCh38#23648060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12427959-C-A

23648060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12427959-C-T

23648270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12428135-G-A

23648330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 12428150-T-C

23648564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 12428348-G-T

http://identifiers.org/hco/18/GRCh38#23648688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12428423-C-A

23648688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 12428423-C-G

23648688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 12428423-C-T

http://identifiers.org/hco/18/GRCh38#23648730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12428464-C-A

23648730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 12428464-C-G

23648730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 12428464-C-T

23648736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 12428470-T-C

23648766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 12428501-G-A

23648766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 12428501-G-T

23648843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 12428702-C-G

23648843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 12428702-C-T

23648853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 12428714-T-C

23648856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 12428717-T-G

23648872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant
orthologous variants: 12428733-T-C

http://identifiers.org/hco/18/GRCh38#23648892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12428747-C-A

23648892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 12428747-C-G

23648892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 12428747-C-T

23648903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 12428758-G-T

23648907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 12428762-T-A

23648907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 12428762-T-C

http://identifiers.org/hco/18/GRCh38#23648912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12428766-C-A

23648912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 12428766-C-T

23648953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 12428808-A-G

23648958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 12428813-G-T

23648978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 12428833-G-T

23649072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 12428923-A-G

23649072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 12428923-A-T

23649122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 12428975-C-T

23649425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12429269-A-G

23649432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12429276-A-G

http://identifiers.org/hco/18/GRCh38#23649434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12429278-C-A

23649434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12429278-C-G

http://identifiers.org/hco/18/GRCh38#23649436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12429280-A-C

23649436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12429280-A-G

23649446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12429290-A-G

23649595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12429441-T-C

23649595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12429441-T-G

http://identifiers.org/hco/18/GRCh38#23651020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12431075-A-C

23651175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12431223-C-T

23651246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12431292-A-G

23651249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12431295-T-C

23651262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12431323-A-T

23651335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12431395-G-A

23651756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12431963-C-G

23652106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12433185-C-T

23652212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12433283-C-T

23652420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12433485-T-C

23652482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12433544-C-T

http://identifiers.org/hco/18/GRCh38#23652502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12433564-C-A

http://identifiers.org/hco/18/GRCh38#23656457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12435552-A-C

23656925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12435979-G-C

23656971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12436026-G-A

23660899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12436924-C-G

23661095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12437100-C-T

23661708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12437666-T-C

23662008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12438108-C-G

23662008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12438108-C-T

23662404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12438529-G-A

http://identifiers.org/hco/18/GRCh38#23662640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12438609-C-A

23662640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12438609-C-G

23662640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12438609-C-T

http://identifiers.org/hco/18/GRCh38#23662644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12438613-C-A

23662644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12438613-C-T

http://identifiers.org/hco/18/GRCh38#23662653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12438622-C-A

23662653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12438622-C-T

http://identifiers.org/hco/18/GRCh38#23662682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12438648-C-A

23662682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12438648-C-G

23662682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12438648-C-T

23662700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12438658-G-A

23662700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12438658-G-C

23662700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: intron variant
orthologous variants: 12438658-G-T

http://identifiers.org/hco/18/GRCh38#23662729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: start lost
orthologous variants: http://identifiers.org/mco/18/GRCm39#12438687-A-C

23662729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: start lost
orthologous variants: 12438687-A-G

23662729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: start lost
orthologous variants: 12438687-A-T

23662781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5 prime UTR variant
orthologous variants: 12438722-T-C

23662781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5 prime UTR variant
orthologous variants: 12438722-T-G

http://identifiers.org/hco/18/GRCh38#23662787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12438728-C-A

23662787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5 prime UTR variant
orthologous variants: 12438728-C-G

23662787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5 prime UTR variant
orthologous variants: 12438728-C-T

http://identifiers.org/hco/18/GRCh38#23662846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#12438768-C-A

23662846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27110
most severe consequence: 5 prime UTR variant
orthologous variants: 12438768-C-T