97737289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 42159192-C-G

97737289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 42159192-C-T

http://identifiers.org/hco/10/GRCh38#97737319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#42159222-C-A

97737319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 42159222-C-T

http://identifiers.org/hco/10/GRCh38#97737399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#42159305-C-A

97737399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42159305-C-G

97737399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42159305-C-T

97737427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42159333-G-A

97737427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42159333-G-T

97737428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42159334-C-T

http://identifiers.org/hco/10/GRCh38#97737463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42159361-A-C

97737463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42159361-A-G

97738332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42159783-A-G

http://identifiers.org/hco/10/GRCh38#97738368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42159876-C-A

97738368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42159876-C-G

97738368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42159876-C-T

97738413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42159918-G-A

97738413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42159918-G-C

97738447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42159958-T-C

97738460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42159971-A-T

97738468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42159976-T-C

97738516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42160024-G-A

http://identifiers.org/hco/10/GRCh38#97738553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42160061-C-A

97738553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42160061-C-T

97738699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42160205-G-T

http://identifiers.org/hco/10/GRCh38#97738707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42160214-C-A

97738939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42160435-T-C

http://identifiers.org/hco/10/GRCh38#97738958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42160447-C-A

97738958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42160447-C-G

97738958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42160447-C-T

97739131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42160557-G-T

http://identifiers.org/hco/10/GRCh38#97739225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42160672-C-A

97739225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42160672-C-G

97739225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42160672-C-T

97739349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42160805-G-T

97739365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42160822-A-G

97739368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42160899-C-T

97739483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42161013-A-G

97739542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42161956-A-G

97739863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42162282-A-T

97739923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42162331-T-A

97740018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42162573-G-A

http://identifiers.org/hco/10/GRCh38#97740165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42162711-A-C

97740225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42162765-T-C

97740238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42162792-A-G

97740255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42162849-G-T

97740367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42162959-G-A

97740392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42162977-G-T

97740672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42163237-G-C

97740739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42163299-C-T

97740883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42163430-C-G

97742711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42165457-T-G

97743042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42165778-C-G

97743042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42165778-C-T

http://identifiers.org/hco/10/GRCh38#97743266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42165993-C-A

97743266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42165993-C-G

97743271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42165994-G-T

97743436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42166144-A-G

97743451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42166166-G-A

97743987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42166726-G-A

97743987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42166726-G-T

97744302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42167119-G-C

97744381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42167203-C-G

http://identifiers.org/hco/10/GRCh38#97744576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42167600-A-C

97744578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42167602-T-A

97744578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42167602-T-C

http://identifiers.org/hco/10/GRCh38#97744639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42167662-A-C

97744643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42167666-G-T

http://identifiers.org/hco/10/GRCh38#97744657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42167675-A-C

97744657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42167675-A-T

97744677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42167693-G-A

97744677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42167693-G-T

97744760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 42167759-T-A

97744760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 42167759-T-C

97744828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42167827-T-C

97744828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42167827-T-G

97744944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42167958-G-T

97744965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42167974-A-G

97745046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42168030-T-G

http://identifiers.org/hco/10/GRCh38#97745049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42168033-C-A

97745049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42168033-C-G

97745049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42168033-C-T

97746995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42168855-A-G

http://identifiers.org/hco/10/GRCh38#97747383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42169249-A-C

97747383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42169249-A-G

http://identifiers.org/hco/10/GRCh38#97747444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42169309-A-C

97747444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42169309-A-T

97747481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42169346-A-G

97747629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42169490-A-G

97747718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42169586-C-T

http://identifiers.org/hco/10/GRCh38#97748119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42169787-C-A

97748119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42169787-C-T

97748217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42169849-C-T

97748396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42170071-T-C

97748485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42170164-G-A

97749069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42170665-A-G

97749326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42170904-T-C

97749326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42170904-T-G

97749382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42170953-G-A

97749422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42170979-C-T

http://identifiers.org/hco/10/GRCh38#97749537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42171161-C-A

97749537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42171161-C-T

97749561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42171185-T-C

97749595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42171219-T-C

http://identifiers.org/hco/10/GRCh38#97749618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42171250-C-A

http://identifiers.org/hco/10/GRCh38#97749799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42171425-C-A

97749855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42171469-G-A

97749942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42171554-T-A

97749942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42171554-T-C

97749942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42171554-T-G

97749969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42171575-G-C

97749969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42171575-G-T

97750141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42171705-T-C

97750141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42171705-T-G

97750264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42171803-T-C

http://identifiers.org/hco/10/GRCh38#97750277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42171816-C-A

97750277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42171816-C-G

97750277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42171816-C-T

97750293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42171832-A-T

97750362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42171898-G-C

97750362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42171898-G-T

http://identifiers.org/hco/10/GRCh38#97750376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42171912-A-C

http://identifiers.org/hco/10/GRCh38#97751064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42172257-C-A

97751181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42172336-G-A

http://identifiers.org/hco/10/GRCh38#97751251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42172402-C-A

97751251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42172402-C-T

97751399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42172565-A-G

97751488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42172654-C-G

97751571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42172741-G-A

http://identifiers.org/hco/10/GRCh38#97751606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42172774-A-C

97751606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42172774-A-G

97751656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42172807-C-T

97751685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42172835-C-T

97751686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42172836-G-A

97751686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42172836-G-T

97751785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42172910-A-G

97751818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42172943-G-A

97752314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42173618-C-T

97752332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42173635-A-T

97752341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42173644-C-G

97752341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42173644-C-T

97752376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42173670-A-G

97752561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42173839-G-A

97752587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42173865-C-T

http://identifiers.org/hco/10/GRCh38#97752705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42173931-C-A

97752705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42173931-C-T

97752904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42174105-A-T

97752926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42174133-G-A

97752972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42174179-G-A

97752972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42174179-G-C

97753044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42174250-G-C

97753063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42174269-C-T

97753145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42174351-G-A

97753145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42174351-G-T

http://identifiers.org/hco/10/GRCh38#97753253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42174462-C-A

97753253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42174462-C-G

97753253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42174462-C-T

97753277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42174487-G-C

97753597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42174707-C-T

http://identifiers.org/hco/10/GRCh38#97753679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42174766-C-A

97753703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42174785-A-G

97753763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42174843-C-G

97753763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42174843-C-T

97753848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42174923-A-G

97754139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42175201-G-T

97754152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42175217-A-G

97754194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42175260-C-T

http://identifiers.org/hco/10/GRCh38#97754295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42175352-C-A

97754295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42175352-C-T

97754659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42175405-T-C

97754709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42175438-A-G

97754725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 42175448-A-G

97754766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42175488-C-G

97754766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42175488-C-T

97754793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42175498-T-A

97754805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42175510-G-A

97754863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42175566-T-G

97754939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42175626-G-T

97755034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42175718-G-A

97755034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42175718-G-T

97755063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42175748-C-T

97755070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42175755-A-G

97755095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42175780-C-T

97755204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42175855-A-G

97755211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42175870-C-G

97755211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42175870-C-T

97755250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42175906-G-A

97755699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42176319-G-A

97756146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42176661-C-T

97756171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42176674-G-A

97756171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42176674-G-T

97756491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42176962-C-T

97756526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42176995-C-T

97756591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42177048-T-A

http://identifiers.org/hco/10/GRCh38#97757104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42177497-C-A

97757147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42177513-G-A

97757147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42177513-G-C

97757147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42177513-G-T

97757220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42177591-A-G

97757235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42177606-G-A

97757269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42177640-C-T

97757284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42177655-G-A

97757284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42177655-G-C

97757290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42177661-C-T

97757331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42177695-C-T

97757339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42177703-G-A

97757339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42177703-G-T

97757345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42177709-A-G

http://identifiers.org/hco/10/GRCh38#97757412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42177782-C-A

http://identifiers.org/hco/10/GRCh38#97758039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42178143-C-A

97758136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 42178227-A-G

http://identifiers.org/hco/10/GRCh38#97758235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42178336-C-A

97758235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42178336-C-T

http://identifiers.org/hco/10/GRCh38#97758239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42178340-C-A

97758239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42178340-C-G

97758239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42178340-C-T

97758264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42178370-T-A

97758264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42178370-T-C

97758264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42178370-T-G

97759162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42178748-G-A

97759162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42178748-G-C

97759162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42178748-G-T

97759215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42178801-C-T

97759270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42178856-T-C

http://identifiers.org/hco/10/GRCh38#97759525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42179060-C-A

97759525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179060-C-T

97759538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179072-G-A

97759538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179072-G-C

97759538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179072-G-T

97759588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179117-G-A

97759588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179117-G-T

97759615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179144-A-G

97759648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179178-G-A

97759648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179178-G-T

97759649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179179-A-T

97759672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179202-T-A

97759672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179202-T-C

97759672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179202-T-G

97759674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179204-G-A

97759674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179204-G-T

http://identifiers.org/hco/10/GRCh38#97759743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42179272-C-A

97759743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179272-C-G

97759743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179272-C-T

97759760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179289-G-T

97760069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179476-G-T

97760217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179614-G-A

97760217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179614-G-T

http://identifiers.org/hco/10/GRCh38#97760302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42179678-C-A

97760430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179784-T-C

97760623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179954-G-A

http://identifiers.org/hco/10/GRCh38#97760659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42179971-C-A

97760659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42179971-C-T

http://identifiers.org/hco/10/GRCh38#97760726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42180015-C-A

97760726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26559
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42180015-C-T