98189990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573086-G-A

98189997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573093-T-C

98190047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573143-T-C

http://identifiers.org/hco/8/GRCh38#98190059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34573155-C-A

98190086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573191-A-T

http://identifiers.org/hco/8/GRCh38#98190145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34573252-C-A

98190185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573270-T-C

98190186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573271-G-A

98190234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573322-C-T

http://identifiers.org/hco/8/GRCh38#98190253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34573343-C-A

98190253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573343-C-T

98190311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573401-G-C

98190311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573401-G-T

98190319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573409-T-A

98190319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573409-T-C

98190658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573448-T-C

http://identifiers.org/hco/8/GRCh38#98190667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34573457-C-A

98190667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573457-C-T

98190679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573469-G-A

98190679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573469-G-T

http://identifiers.org/hco/8/GRCh38#98190720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34573511-C-A

98190720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573511-C-T

98190775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573552-T-C

http://identifiers.org/hco/8/GRCh38#98190861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34573639-C-A

98191003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573785-T-A

98191005-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34573787-T-G

http://identifiers.org/hco/8/GRCh38#98191384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34574136-C-A

98191509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34574218-G-A

98191509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34574218-G-T

98191964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34574657-G-T

98192083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34574787-C-T

http://identifiers.org/hco/8/GRCh38#98192165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34574875-C-A

http://identifiers.org/hco/8/GRCh38#98192477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34575126-C-A

98192477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34575126-C-G

98192495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34575141-T-G

http://identifiers.org/hco/8/GRCh38#98192528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34575173-A-C

98192528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34575173-A-G

98192536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34575181-T-A

98192536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34575181-T-G

98192635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34575277-G-T

http://identifiers.org/hco/8/GRCh38#98192718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34575360-A-C

98192719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34575361-G-A

98192719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34575361-G-T

98193203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34575829-G-A

98193203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34575829-G-T

98193303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34575926-A-G

98193364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34575974-T-G

98193373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34575983-G-A

98193485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34576064-G-A

98193485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34576064-G-C

98193493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34576072-T-A

98193493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34576072-T-G

98193983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34576289-C-T

98194086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34576373-G-T

http://identifiers.org/hco/8/GRCh38#98194577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34576739-A-C

98194577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34576739-A-G

98194607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34576765-T-C

98194613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34576769-G-A

98194613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34576769-G-T

98194737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34577725-T-C

98194737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34577725-T-G

98194768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34577756-T-C

98194833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34577821-A-G

98194874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34577861-G-A

98194874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34577861-G-T

98194922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34577909-T-A

98194923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34577910-G-A

98194923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34577910-G-T

http://identifiers.org/hco/8/GRCh38#98194936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34577923-C-A

98194936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34577923-C-T

http://identifiers.org/hco/8/GRCh38#98195137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34578130-C-A

http://identifiers.org/hco/8/GRCh38#98195616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34578585-C-A

98195637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34578606-G-T

98195713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34578666-T-A

98195713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34578666-T-C

98195713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34578666-T-G

http://identifiers.org/hco/8/GRCh38#98195740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34578694-C-A

http://identifiers.org/hco/8/GRCh38#98195771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34578725-C-A

98195771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34578725-C-T

98195777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34578729-G-A

98195777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34578729-G-T

http://identifiers.org/hco/8/GRCh38#98195779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34578731-C-A

98195779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34578731-C-G

98195779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34578731-C-T

98195807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34578759-T-A

98195807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34578759-T-C

http://identifiers.org/hco/8/GRCh38#98195854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34578778-C-A

98195854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34578778-C-T

98196047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34578956-G-A

98196047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34578956-G-T

98196067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34578976-T-A

98196092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34579002-T-C

http://identifiers.org/hco/8/GRCh38#98196272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34579428-C-A

98196272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34579428-C-G

98196444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34579584-C-T

98196679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34579824-T-C

98196768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34579921-A-G

98197063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34580197-G-T

98197107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34580210-C-T

98197124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34580227-A-T

98201283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34581774-C-T

98201377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34581859-A-G

98201450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34581883-C-T

http://identifiers.org/hco/8/GRCh38#98201668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34581920-C-A

98201781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34582038-C-T

98201819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34582086-T-A

98201992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34582225-G-A

98202155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34582379-A-G

98202158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34582382-G-T

98202203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34582413-A-G

98203282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34583038-T-C

http://identifiers.org/hco/8/GRCh38#98203345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34583100-C-A

98203432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34583187-T-A

98203763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34583498-A-T

98203880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34583665-A-G

98203905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34583690-A-T

98203908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34583693-G-T

98203913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34583698-T-C

98204036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34583794-T-C

98204212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34583964-A-G

98204367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584061-A-G

98204650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584334-T-G

98204866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584548-G-A

98204912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584593-G-A

98204912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584593-G-T

98205025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584701-A-G

98205025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584701-A-T

http://identifiers.org/hco/8/GRCh38#98205100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34584765-A-C

98205289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584944-G-T

98205291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584946-T-C

98205312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584971-G-A

98205312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34584971-G-T

98205678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585298-G-T

98205700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34585317-C-T

http://identifiers.org/hco/8/GRCh38#98205898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34585454-C-A

98207696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34587114-C-G

98207777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34587196-G-T

98207852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34587248-C-T

98208243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34587640-C-T

98210912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34598996-T-C

98211034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34599105-G-A

98211062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34599134-T-C

98211214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34599268-A-G

98212295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34600097-A-G

http://identifiers.org/hco/8/GRCh38#98212303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34600105-A-C

98212303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34600105-A-G

98212307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34600109-A-G

98212308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34600110-T-A

98212308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34600110-T-C

98212308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34600110-T-G

98212309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34600111-G-C

98212309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34600111-G-T

98212393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34600149-A-G

98212557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34600317-G-T

http://identifiers.org/hco/8/GRCh38#98212568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34600328-C-A

98212568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34600328-C-T

98212628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34600385-G-T

http://identifiers.org/hco/8/GRCh38#98212734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34600490-A-C

98212795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34600545-C-T

98215392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34602579-T-A

98215463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34602641-C-T

98215575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34602697-A-G

98216216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34604036-C-T

98216296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34604115-C-T

98216446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34604268-A-G

98216585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34604399-G-A

98216688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34604492-T-A

98216970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34604752-T-C

98216970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34604752-T-G

98217052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34604829-G-C

98217052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34604829-G-T

98217089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34604873-G-A

98217089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34604873-G-T

98217168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34604960-T-C

98217168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34604960-T-G

98217279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34605064-A-G

98217291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34605073-G-A

98217291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34605073-G-T

98217306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34605088-A-G

98217361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34605130-G-T

98217365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34605134-A-G

98217375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34605144-G-T

98217482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34605259-G-T

98217742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34605670-G-A

98218472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34606634-C-T

98218569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34606723-T-C

98218624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34606777-G-A

98218624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34606777-G-T

98218826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34607029-C-G

98218926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34607149-G-C

98218963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34607186-G-C

98219031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34607252-T-C

98219031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34607252-T-G

98219145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34607356-G-A

98219189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34607403-G-A

98219232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34607451-T-C

http://identifiers.org/hco/8/GRCh38#98220086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34608295-A-C

98220159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34608358-C-G

98220160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34608359-A-G

98222371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34609211-A-G

http://identifiers.org/hco/8/GRCh38#98222381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34609220-A-C

98222381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34609220-A-T

98222547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34609387-T-C

98222560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34609400-G-A

98222628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34609468-A-G

98222716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34609703-T-A

98222716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34609703-T-G

98222722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34609709-T-A

98222725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34609734-G-A

98222725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34609734-G-T

http://identifiers.org/hco/8/GRCh38#98222741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34609750-C-A

98222741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34609750-C-G

98222789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34609781-T-G

98223073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34610062-T-C

http://identifiers.org/hco/8/GRCh38#98223263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34610228-C-A

98223439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34610375-T-C

98223553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34610663-C-T

98223774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34610871-G-A

98223934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34611041-T-C

98224023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34611143-A-G

http://identifiers.org/hco/8/GRCh38#98224034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34611154-A-C

98224034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34611154-A-G

http://identifiers.org/hco/8/GRCh38#98224204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34611326-A-C

98224225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34611357-A-G

98224234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34611366-G-T

98224251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34611383-C-T

98228552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34613763-C-T

98228684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34613855-A-G

98228685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34613856-G-T

98228716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34613880-A-G

98229225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34614756-A-G

98229235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34614766-T-C

98229333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34614857-C-T

98231056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34615772-T-G

98231636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34616871-A-G

98231664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34616909-A-G

http://identifiers.org/hco/8/GRCh38#98231696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34616948-C-A

98231696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34616948-C-T

98231836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34617088-G-A

http://identifiers.org/hco/8/GRCh38#98231884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34617137-C-A

98231884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34617137-C-T

98231897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34617150-T-C

98231969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34617223-G-A

98232117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34617342-A-G

98232136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34617359-T-G

98232275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34617486-C-T

98232315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34617520-C-T

98232936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34618026-A-G

98235428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34624673-A-T

98235500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34624744-C-G

98235615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34624855-G-T

98236023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34624996-T-A

98236023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34624996-T-C

98236023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34624996-T-G

http://identifiers.org/hco/8/GRCh38#98236101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34625065-A-C

98236101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34625065-A-G

98236194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34625157-T-C

98237548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34625710-C-T

http://identifiers.org/hco/8/GRCh38#98237553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34625715-C-A

98237784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34625946-T-C

98237840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34625991-C-T

98237924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34626051-T-C

98238295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34626301-G-A

98238334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34626330-G-A

98238390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34626378-T-A

http://identifiers.org/hco/8/GRCh38#98238505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34626487-A-C

98238603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34626590-G-T

98238625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34626596-C-T

98238723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34626691-G-C

http://identifiers.org/hco/8/GRCh38#98238953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34628545-A-C

98239184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34628729-C-T

http://identifiers.org/hco/8/GRCh38#98239204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34628749-A-C

98239289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34628831-C-G

98239481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34629006-C-T

http://identifiers.org/hco/8/GRCh38#98239690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34629633-C-A

98239782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34629705-C-T

98239789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34629712-C-T

98239839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34629762-G-C

98239992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34629914-T-C

98240080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34629993-A-T

http://identifiers.org/hco/8/GRCh38#98240291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34630872-C-A

http://identifiers.org/hco/8/GRCh38#98240378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34630955-A-C

98240380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34630957-T-C

98240576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34631137-T-A

98240684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34631240-G-A

98240771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34631319-C-T

98240895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34631437-A-G

98241238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34631740-A-G

98241679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34632147-G-A

98241818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34632273-G-A

98242967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34632867-G-A

98243694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34634697-G-A

98243702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34634706-T-C

98243933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34634979-G-A

98243975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34635020-A-G

98244577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34635327-T-G

http://identifiers.org/hco/8/GRCh38#98244616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34635384-C-A

98244616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34635384-C-G

98244616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34635384-C-T

98244732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34635511-C-T

98244733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34635512-A-G

98245085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34635872-A-G

98245154-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34635939-A-T

98245205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34635989-C-G

98245273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34636057-C-T

98245309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34636092-C-T

98246449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34637237-G-A

98246582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34637377-C-T

98246615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34637412-T-A

98246764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34637548-A-G

98246790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34637574-T-C

98246843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34637614-C-T

98246872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34637639-T-C

98246983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34637746-G-A

http://identifiers.org/hco/8/GRCh38#98247106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34637867-C-A

98247106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34637867-C-T

98247107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34637868-C-T

98247139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34637900-G-A

98248339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639146-A-G

98248548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639348-G-T

98248588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639388-C-G

98248893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639626-G-A

98248941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639666-C-G

98248942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639667-G-A

98248952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639677-T-C

98248984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639751-C-T

98249227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34639936-G-T

98251118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34646674-C-T

98251164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34646713-A-G

98251292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34646830-A-G

http://identifiers.org/hco/8/GRCh38#98251351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34646884-C-A

98251351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34646884-C-T

98251462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34646950-G-A

http://identifiers.org/hco/8/GRCh38#98251468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34646956-C-A

98251563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34647789-G-A

98251563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34647789-G-T

98251664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34647896-G-T

98251693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34647924-T-C

98251748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34647952-T-C

98252209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34648582-G-A

98252209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34648582-G-T

98252246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34648622-A-G

98252246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34648622-A-T

98252257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34648633-A-G

98252257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34648633-A-T

98252287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34648663-A-G

98252363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34648735-T-C

98252491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34648840-G-A

98252491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34648840-G-T

98253377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34650196-T-C

98253980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34650492-A-T

98253997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34650507-G-T

98254116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34650631-A-G

98254396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34651200-A-G

http://identifiers.org/hco/8/GRCh38#98254612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34651388-A-C

98255026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34651777-G-A

98255987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34653073-T-A

98255987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34653073-T-C

98278933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34663500-G-A

98279018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34663572-G-C

98279202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34664426-C-G

98279226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34664450-T-C

http://identifiers.org/hco/8/GRCh38#98279276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34664500-C-A

98279481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34664689-C-T

98279572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34664769-G-T

98279580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34664777-T-C

98279580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34664777-T-G

98279632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34664858-G-A

98279800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34665013-A-T

98279912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34665106-G-T

98280102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34665492-G-A

http://identifiers.org/hco/8/GRCh38#98280444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34665796-C-A

98280703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34665957-A-G

98280812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34666021-T-A

98281938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34666817-G-A

98281938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34666817-G-T

98282257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34667114-C-T

http://identifiers.org/hco/8/GRCh38#98282934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34667914-C-A

98283184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34668182-T-C

http://identifiers.org/hco/8/GRCh38#98283705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34668544-A-C

98283887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34668716-T-G

98283899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34668728-C-T

98284117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34668946-G-A

98284248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34669179-A-G

98284970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34670279-G-A

98289147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34671177-C-T

98289224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34671243-T-C

98289225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34671244-T-C

98289242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34671263-C-T

98289531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34671465-T-C

98289737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34671581-A-G

http://identifiers.org/hco/8/GRCh38#98290018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34671857-C-A

98290044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34671882-G-C

98290288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34672130-A-G

98290399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34672230-A-G

98290440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34672269-C-T

http://identifiers.org/hco/8/GRCh38#98290479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34672308-C-A

98290479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34672308-C-T

98291133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34676161-G-A

http://identifiers.org/hco/8/GRCh38#98291164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34676190-A-C

98291217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34676243-C-T

98291363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34676374-C-G

98291889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34676803-C-G

98291975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34676878-A-G

98292159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34677039-G-A

http://identifiers.org/hco/8/GRCh38#98292837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34677682-A-C

98293128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34677934-G-A

98293128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34677934-G-C

98293128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34677934-G-T

http://identifiers.org/hco/8/GRCh38#98293551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34678310-A-C

98293839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34678559-C-T

98293893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34678607-G-A

98293893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34678607-G-T

http://identifiers.org/hco/8/GRCh38#98294023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#34678725-C-A

98294023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34678725-C-T

98294039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34678741-G-A

98294039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34678741-G-T

98294069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 34678771-A-G

98294069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34678771-A-T

98294195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34678891-G-A

98294195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25854
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34678891-G-T