123768515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 58287390-T-A

123768515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 58287390-T-C

123768516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 58287391-C-G

123768516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 58287391-C-T

123768945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58287696-G-C

123768990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58287720-A-G

123769200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58287873-C-T

123769514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58288160-G-A

http://identifiers.org/hco/8/GRCh38#123769536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58288178-A-C

123769817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58288439-A-G

123771137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58289192-C-T

123771168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58289215-T-C

123771553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58289728-A-G

123771876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58290100-G-C

123772038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58290243-G-A

123772402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58290612-G-A

123773271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58290861-T-C

123774161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 58292129-T-C

123774161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 58292129-T-G

123774933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58293390-C-T

123774957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58293411-A-G

123775229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 58293677-C-T

http://identifiers.org/hco/8/GRCh38#123775388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58293794-C-A

123775388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58293794-C-T

123775458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58293852-G-A

123776740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58294700-C-T

http://identifiers.org/hco/8/GRCh38#123777417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58295310-A-C

123777451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58295372-A-G

123777451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58295372-A-T

123777459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58295379-G-T

123777626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58295643-A-G

123777626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58295643-A-T

http://identifiers.org/hco/8/GRCh38#123777795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58295815-C-A

123777807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58295827-T-A

123778117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58296145-T-C

123778213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58296233-A-G

http://identifiers.org/hco/8/GRCh38#123778219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58296239-C-A

123778219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58296239-C-T

123778340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58296351-C-T

123778727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 58296694-G-A

123779021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58297520-G-A

123779371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58297849-A-G

123779525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58297999-C-T

123779701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58298153-A-G

123780163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58298609-T-A

123780225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58298670-T-A

http://identifiers.org/hco/8/GRCh38#123780448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58298872-C-A

123780448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58298872-C-G

123780448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58298872-C-T

http://identifiers.org/hco/8/GRCh38#123780449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58298873-C-A

123780449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58298873-C-T

123780450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58298874-A-G

123780647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58299092-A-G

http://identifiers.org/hco/8/GRCh38#123780692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58299128-C-A

123780692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58299128-C-G

123781339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58299420-G-C

http://identifiers.org/hco/8/GRCh38#123783938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58301390-A-C

123784046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58301468-C-T

123784130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58301544-A-G

123784179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58301575-T-C

123784289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58301676-G-A

123784340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58301717-G-A

123784367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58301744-G-A

123784367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58301744-G-T

http://identifiers.org/hco/8/GRCh38#123784369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58301746-C-A

123784369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58301746-C-T

123785396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58302339-C-G

123785510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58302417-G-A

http://identifiers.org/hco/8/GRCh38#123785583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58302475-C-A

123786145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 58302725-A-G

123786435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58302995-T-C

123786747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58303310-G-T

http://identifiers.org/hco/8/GRCh38#123787130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58304234-C-A

123787274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 58304377-T-C

123787767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58304849-T-A

123787767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58304849-T-C

123787811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58304877-G-A

http://identifiers.org/hco/8/GRCh38#123787817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58304887-C-A

123787817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58304887-C-G

123787900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58304968-A-G

http://identifiers.org/hco/8/GRCh38#123788017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58305075-A-C

123788060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58305114-G-A

123788220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 58305236-A-G

http://identifiers.org/hco/8/GRCh38#123788336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58305315-C-A

123788390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58305361-C-T

123788572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58305541-T-A

123788595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58305564-C-G

123789779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58306670-T-A

123792685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58307464-A-G

123792746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58307525-C-T

123797906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58312970-A-G

123798337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58313615-T-C

123798373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58313648-G-T

123798515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58313789-G-A

123798679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58313924-A-G

123798753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58313995-G-A

123798864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58314106-A-G

123799109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58314291-G-A

123799265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58314425-T-C

123799420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58314575-G-A

http://identifiers.org/hco/8/GRCh38#123799479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58314635-C-A

123799479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58314635-C-G

123799837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 58315075-G-C

123799837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 58315075-G-T

123804960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58319152-C-T

123805065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58319248-T-C

123805230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58319407-G-C

123805230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58319407-G-T

123805359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58319526-T-A

123805359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58319526-T-C

123805393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58319550-G-A

123805393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58319550-G-T

123806012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58320127-T-A

http://identifiers.org/hco/8/GRCh38#123806088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58320200-C-A

123806088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 58320200-C-G

123806088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 58320200-C-T

123806305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58320377-G-T

123806588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58320522-G-A

123806809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58320610-A-G

http://identifiers.org/hco/8/GRCh38#123806979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58320708-A-C

123807461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58321011-G-T

http://identifiers.org/hco/8/GRCh38#123807470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58321018-C-A

123807470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58321018-C-G

123807470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58321018-C-T

http://identifiers.org/hco/8/GRCh38#123807967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58321431-A-C

123807967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58321431-A-G

123808235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58321741-T-C

http://identifiers.org/hco/8/GRCh38#123808277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58321785-C-A

123808277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 58321785-C-G

123808421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58321926-A-G

http://identifiers.org/hco/8/GRCh38#123808479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58321977-C-A

123808479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58321977-C-T

123808504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58322006-G-T

123808666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 58322179-G-T

http://identifiers.org/hco/8/GRCh38#123808728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58322242-C-A

123808999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 58322493-C-G

123809477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58323061-T-C

123809648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58323197-C-T

123809742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58323272-C-T

123809782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58323303-A-G

123810402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58324952-G-A

123810402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58324952-G-T

http://identifiers.org/hco/8/GRCh38#123810403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58324956-C-A

http://identifiers.org/hco/8/GRCh38#123810405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58324958-C-A

123810407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58324960-A-G

123810496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58325019-A-G

123810543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58325066-A-G

http://identifiers.org/hco/8/GRCh38#123810651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58325170-C-A

123810692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58325202-T-C

123810764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58325230-A-G

http://identifiers.org/hco/8/GRCh38#123810772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58325238-C-A

123810772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58325238-C-T

http://identifiers.org/hco/8/GRCh38#123810789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58325257-C-A

123810789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58325257-C-T

http://identifiers.org/hco/8/GRCh38#123811373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58325977-C-A

123811375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58325979-A-G

http://identifiers.org/hco/8/GRCh38#123811454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58326065-C-A

123811454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58326065-C-T

123811499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58326104-A-G

123811618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58326188-T-A

123811779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58326312-G-A

123811779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58326312-G-C

123811779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58326312-G-T

123812393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58326496-T-C

123812393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58326496-T-G

http://identifiers.org/hco/8/GRCh38#123812428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58326524-C-A

123812428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58326524-C-G

123812428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58326524-C-T

http://identifiers.org/hco/8/GRCh38#123812429-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58326525-A-C

123812429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58326525-A-G

123812429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58326525-A-T

http://identifiers.org/hco/8/GRCh38#123812547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58326627-C-A

123812547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58326627-C-T

123812588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58326668-G-A

123812588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58326668-G-C

123812705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 58326785-T-A

123813151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327223-T-A

123813151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327223-T-C

123813223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327293-T-C

123813284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327354-G-T

123813402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327466-A-G

123813451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327514-A-G

123813451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327514-A-T

123813552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327618-T-C

123813619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327680-C-T

123813635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327696-C-T

123813678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327727-A-G

123813689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327735-A-T

123813809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327847-T-C

123813828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327857-A-G

http://identifiers.org/hco/8/GRCh38#123813885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58327878-C-A

123813924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58327914-G-T

http://identifiers.org/hco/8/GRCh38#123813945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58327935-C-A

123814123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58328118-G-A

123814559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58328539-A-G

123814687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58328671-G-A

123814687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 58328671-G-C

http://identifiers.org/hco/8/GRCh38#123814859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58328806-A-C

123814944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3 prime UTR variant
orthologous variants: 58328894-G-T

123815058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3 prime UTR variant
orthologous variants: 58328988-T-C

123815084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26306
most severe consequence: 3 prime UTR variant
orthologous variants: 58329014-C-T