20100955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30430414-T-C

20101201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30430206-T-C

20101229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30430178-G-A

http://identifiers.org/hco/6/GRCh38#20101267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30430143-A-C

http://identifiers.org/hco/6/GRCh38#20101277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30430133-C-A

20101552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30429817-T-C

20101567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30429802-T-G

20101733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30429669-T-C

20102146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30429579-T-A

20102146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30429579-T-C

20102146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30429579-T-G

20102198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30429536-T-A

20102229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30429507-G-C

20102229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30429507-G-T

http://identifiers.org/hco/6/GRCh38#20102247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30429489-C-A

20102247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30429489-C-G

20102247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30429489-C-T

20102261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30429476-G-A

20102322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30429417-C-G

20102329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30429410-C-T

20102416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30429326-G-T

20102438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30429306-A-G

20102458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30429286-G-A

20102506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30429242-G-A

20102506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30429242-G-C

20102506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30429242-G-T

20102518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30429229-G-A

20102518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30429229-G-C

20102518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30429229-G-T

20102697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30429094-T-C

20104436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30428691-T-C

20104446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30428681-A-T

20104576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30428567-A-T

20105195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30426817-C-T

20106161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425949-A-G

20109409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425482-G-A

20109426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425465-T-C

20109464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425427-T-A

20109467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425424-G-A

20109467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425424-G-T

http://identifiers.org/hco/6/GRCh38#20109488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30425404-C-A

20109488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425404-C-T

20109640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30425254-G-A

20109688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30425206-G-A

20109773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425122-T-C

20109773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425122-T-G

http://identifiers.org/hco/6/GRCh38#20109781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30425115-A-C

20109784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425112-G-A

http://identifiers.org/hco/6/GRCh38#20109812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30425086-C-A

20109812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425086-C-G

20109814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425084-G-A

20109814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425084-G-C

20109855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425056-G-A

20109855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425056-G-C

20109855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425056-G-T

http://identifiers.org/hco/6/GRCh38#20109860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30425051-C-A

20109860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425051-C-T

http://identifiers.org/hco/6/GRCh38#20109889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30425021-A-C

http://identifiers.org/hco/6/GRCh38#20109897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30425013-C-A

20109897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425013-C-G

20109897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30425013-C-T

http://identifiers.org/hco/6/GRCh38#20110857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30424678-A-C

20110959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30424599-A-T

20111388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30423734-A-G

20111593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30423531-A-G

20111981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30423224-A-G

20112436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30422619-T-C

20112504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30422553-T-C

20112643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30422419-T-C

20112736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30422333-T-G

http://identifiers.org/hco/6/GRCh38#20112784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30422184-C-A

20112784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30422184-C-T

20112789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30422179-C-T

20112796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30422161-C-T

20112804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30422153-G-A

http://identifiers.org/hco/6/GRCh38#20112826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30422121-C-A

20112826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30422121-C-T

20112987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30421965-T-C

20113049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30421902-C-T

20113092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30421860-G-A

20113135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30421818-G-A

20113135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30421818-G-T

20113482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30421481-G-A

20113660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30420813-C-T

20113763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30420713-A-G

http://identifiers.org/hco/6/GRCh38#20113963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30420389-A-C

20113966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30420386-A-G

20114973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30420043-A-G

20115153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30419869-C-T

20115160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30419862-C-T

20115277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30419746-G-A

20115277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30419746-G-T

20115372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30419651-A-T

20115421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30419601-G-A

20115421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30419601-G-T

http://identifiers.org/hco/6/GRCh38#20115914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30419121-C-A

20116512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30418086-G-A

20116512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30418086-G-C

20116512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30418086-G-T

http://identifiers.org/hco/6/GRCh38#20116559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30418039-A-C

20117019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30417706-A-T

20117282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30417483-C-T

20117342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30417416-G-A

20117404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30417351-C-T

20117849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30416738-A-T

20117868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30416720-T-C

20117868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30416720-T-G

20117955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30416629-A-T

20118042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30416543-G-A

20118092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30416401-C-G

20118141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30416346-G-A

20118157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30416330-T-C

20118157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30416330-T-G

20118294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30416183-G-T

20118300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30416177-T-C

20118306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30416171-G-A

20118306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30416171-G-T

20118407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30416081-T-C

20118407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30416081-T-G

20118462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30416023-G-A

http://identifiers.org/hco/6/GRCh38#20118510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30415975-C-A

20118581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30415905-G-T

20118712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30415764-T-C

20118731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30415745-T-G

20118750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30415726-C-T

20118780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30415698-A-G

20118804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30415676-T-A

20118804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30415676-T-C

20118808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30415672-A-G

http://identifiers.org/hco/6/GRCh38#20118939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30415547-A-C

http://identifiers.org/hco/6/GRCh38#20119027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30415466-A-C

20119367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30414664-A-T

20120271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30413280-T-G

20120957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30412891-T-A

20121325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30412536-T-C

20121551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30412320-C-T

20121555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30412316-G-A

20121555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30412316-G-C

20121593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30412289-T-G

20121847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30412027-A-T

20122239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30411837-C-G

20122295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30411759-T-A

20122350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30411731-T-C

20122541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30411558-T-C

20123227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30411085-A-G

20123519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410966-A-G

20123591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410893-G-A

20123591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410893-G-T

http://identifiers.org/hco/6/GRCh38#20123601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30410883-C-A

20124240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410616-T-G

20124250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410606-G-A

20124296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410561-C-G

20124318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410540-G-T

20124326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410529-G-C

20124326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410529-G-T

20124338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410518-C-T

20124339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410517-G-A

20124339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410517-G-C

20124339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410517-G-T

http://identifiers.org/hco/6/GRCh38#20124348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30410508-A-C

20124353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410500-A-G

20124575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30410279-A-G

20124606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 30410248-A-T

20124625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410220-C-T

20124713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410174-T-A

20124745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410136-T-A

20124745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30410136-T-C

20125003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30409921-G-C

20125003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30409921-G-T

20125016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30409909-G-A

20125037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30409887-G-A

20125081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30409845-A-G

20125260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30409323-A-T

20125282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30409307-G-C

20126381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30409213-T-C

20126381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30409213-T-G

20126384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30409210-T-C

http://identifiers.org/hco/6/GRCh38#20126421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30409174-C-A

20126421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30409174-C-T

20126447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30408647-A-T

http://identifiers.org/hco/6/GRCh38#20126456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30408638-C-A

20126456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30408638-C-G

20126456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30408638-C-T

20126458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30408636-T-G

20126516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 30408548-C-T

20126554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30408510-C-T

20126599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30408465-T-C

http://identifiers.org/hco/6/GRCh38#20126839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#30408261-C-A

20126839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408261-C-T

20126847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408253-G-A

20126847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30408253-G-T

20126886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30408215-G-A

20127041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30408069-T-C

20127168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30407940-C-T

20127214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30407897-A-G

20128559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30406755-T-C

20128574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30406740-G-A

20128574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30406740-G-C

20128574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30406740-G-T

http://identifiers.org/hco/6/GRCh38#20128762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30406346-A-C

20128815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30406315-A-G

20129122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30405987-G-A

20129659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30405320-G-A

20129977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404463-G-C

20130029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404413-T-G

20130068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404375-A-G

20130148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404292-A-G

20130195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404256-T-A

20130196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404255-T-C

20130206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404245-C-T

20130229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404224-C-G

20130259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404194-A-G

20130301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30404152-G-A

20131104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30403711-G-T

20131613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30403590-G-A

20131736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30403476-C-T

20131754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30403458-T-C

20133283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30401676-C-T

20133537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30401403-C-G

20134201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30400738-C-T

20134375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30400512-T-C

20134965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30399240-G-A

20134986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30399221-G-A

20134986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30399221-G-T

http://identifiers.org/hco/6/GRCh38#20135233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30398983-A-C

20135233-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30398983-A-T

http://identifiers.org/hco/6/GRCh38#20135268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30398947-C-A

20136461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30398398-A-G

20136634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30398234-G-A

20136749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30398122-C-T

20136857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30398010-A-G

20136935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30397906-G-C

20136965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30397773-C-T

http://identifiers.org/hco/6/GRCh38#20137063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30397671-C-A

20137090-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30397649-T-G

20137116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30397623-C-T

20137177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30397563-T-C

20137276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30397467-C-G

20137276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30397467-C-T

20137500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30397252-C-T

http://identifiers.org/hco/6/GRCh38#20138223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30396187-C-A

20138289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30396115-C-T

20138830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30395276-A-G

20139910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30394845-G-A

20141252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30392568-T-G

20143071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30389116-A-G

20144092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386526-A-G

20144092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386526-A-T

http://identifiers.org/hco/6/GRCh38#20144105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30386513-C-A

20144105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386513-C-T

20144108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386512-C-G

20144108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386512-C-T

20144148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386474-G-A

20144148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386474-G-C

20144158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386464-G-T

20144370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386251-A-G

http://identifiers.org/hco/6/GRCh38#20144374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30386247-A-C

20144374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386247-A-G

20144377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386244-T-G

20144415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386208-G-C

20144415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386208-G-T

20144423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386200-G-A

20144423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386200-G-T

20144440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386183-G-A

20144440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386183-G-C

20144440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386183-G-T

20144456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386157-T-A

20144456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30386157-T-C

http://identifiers.org/hco/6/GRCh38#20146460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30384132-A-C

20146624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30383969-C-G

20146840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30383791-A-T

20146848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30383783-G-C

20147903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30383419-C-T

http://identifiers.org/hco/6/GRCh38#20149118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30382445-A-C

20149139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30382424-T-A

20149300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30382274-C-T

20149433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30381799-T-C

http://identifiers.org/hco/6/GRCh38#20149502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30381751-C-A

20149556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30381670-A-G

20149568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30381662-C-T

20149856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30381405-T-A

20149860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30381401-T-C

20150260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380335-C-T

20150283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380311-T-C

20150404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380203-T-C

20150477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380124-G-A

20150518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380083-G-A

20150518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380083-G-C

20150521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380080-A-G

20150898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380030-T-C

20150900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30380028-T-G

20150929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379999-G-A

20150929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379999-G-C

20150965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379978-T-C

20151054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379876-G-T

20151277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379673-A-T

20151278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379672-G-A

20151278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379672-G-T

20151281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379669-G-A

20151281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379669-G-T

20151288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379662-G-A

20151288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379662-G-T

20151430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379545-A-G

20151707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379202-A-T

20151831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379067-G-C

http://identifiers.org/hco/6/GRCh38#20151860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30379039-C-A

20151860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30379039-C-T

20152003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30378921-G-C

20152024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30378900-T-C

20152459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30378826-G-A

20152495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30378790-A-T

20152513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30378760-T-C

20152522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30378746-T-C

20152572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30378714-G-C

20152572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30378714-G-T

http://identifiers.org/hco/6/GRCh38#20152592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30378694-C-A

20152592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30378694-C-T

20152594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30378692-A-G

20153829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30376761-G-C

20154100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30376465-C-T

20155239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30375432-A-G

20155241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30375430-T-C

20155251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30375420-C-T

20159888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30370772-A-G

20160192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30370440-A-G

20160268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30370366-C-T

http://identifiers.org/hco/6/GRCh38#20160360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30370272-C-A

20160360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30370272-C-T

20160632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30370175-C-T

20160783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30370068-G-T

20160876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30369987-T-A

20161658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30369765-G-A

20161680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30369743-A-G

20161680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30369743-A-T

20161832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30369631-T-C

20161965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30369539-T-G

20162188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30369343-T-G

20162377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30369163-A-G

20162396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30369143-G-C

20162400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30369139-G-A

20162444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30369086-G-A

20162520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30369018-C-T

20162669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30368584-C-T

http://identifiers.org/hco/6/GRCh38#20163060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30368222-C-A

20163343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30368000-G-C

20163379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30367980-A-G

20163506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30367861-A-T

20163594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30367770-G-T

20163837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30366933-T-G

20163875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30366896-T-G

20163916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30366867-A-G

http://identifiers.org/hco/6/GRCh38#20163991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30366797-A-C

20164149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30366647-A-G

20164373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30366470-C-T

20164382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30366461-G-A

http://identifiers.org/hco/6/GRCh38#20164455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30366413-A-C

20164458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30366410-A-G

20164483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30366385-C-T

http://identifiers.org/hco/6/GRCh38#20165782-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30362022-A-C

http://identifiers.org/hco/6/GRCh38#20165812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30361989-C-A

20165812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30361989-C-T

20165915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30361870-A-G

20165932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30361858-G-A

20165932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30361858-G-T

20166010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30361773-T-C

20166457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30360569-G-A

20166500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30360527-T-C

20166500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30360527-T-G

20167029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30360205-A-G

20167417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30359804-G-T

20167562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30359668-C-T

20167619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30359614-G-C

20167881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30359254-T-C

20168066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30359068-G-A

20168121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30359009-T-C

http://identifiers.org/hco/6/GRCh38#20168233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30358896-C-A

20169174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30358437-T-C

20169174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30358437-T-G

20169214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30358397-G-A

20169438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30358174-T-C

20169570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30358048-A-G

20170483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30357027-C-G

20173524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30354243-A-G

20174010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30354034-A-G

20175214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30351810-T-C

20176492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30351510-T-C

20176508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30351494-G-A

20176657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30351335-T-C

20177311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30350751-C-T

20178073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30350458-G-A

20178496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30350051-A-G

20178789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30349585-G-A

20178891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30349389-T-A

http://identifiers.org/hco/6/GRCh38#20180355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30348216-C-A

20180632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30347914-C-G

20180648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30347898-C-T

20180850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30347706-C-G

20181703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30346832-C-G

20181777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30346760-G-A

20181777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30346760-G-C

20181942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30346163-G-T

20181947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30346158-T-C

20182037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30346091-T-C

20182122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30345816-T-C

20182166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30345771-T-A

20182461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30345516-A-G

20186465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30344171-G-A

20186475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30344161-T-A

20186607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30344045-C-T

20186608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30344044-G-A

20186620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30344032-C-T

20186654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30343998-A-G

http://identifiers.org/hco/6/GRCh38#20186707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30343967-C-A

20186810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30343873-T-G

http://identifiers.org/hco/6/GRCh38#20186894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30343793-C-A

20187450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30343031-G-A

20187450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30343031-G-T

20187474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30343009-T-C

20187488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30342995-G-A

http://identifiers.org/hco/6/GRCh38#20187564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30342922-A-C

http://identifiers.org/hco/6/GRCh38#20187568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30342918-A-C

20187936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30342402-G-A

20187936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30342402-G-C

20188013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30342339-A-G

20188117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30342262-T-C

20188374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30342020-A-G

20192190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30340048-A-G

20192214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30340025-A-T

20192237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30340002-C-G

http://identifiers.org/hco/6/GRCh38#20192528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30339734-C-A

20192618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30339555-A-G

20192620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30339553-T-C

20192838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30339405-C-G

20192962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30339283-G-T

20198493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30333742-A-G

20198559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30333658-T-C

20198682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30333540-T-C

http://identifiers.org/hco/6/GRCh38#20198753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30333469-A-C

20200237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30332591-C-T

20200290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30332531-G-A

20200319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30332502-G-A

20200337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30332480-G-A

20200392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30332424-T-G

20201368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30331720-G-T

20201434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30331634-C-T

20201472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30331604-G-A

20201577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30331485-T-C

20201577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30331485-T-G

20201615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30331447-C-T

20201681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30331389-A-G

20201748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30331323-T-C

20201755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30331316-A-G

20201925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30331230-T-A

20202290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30330926-A-G

20202300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30330911-T-G

20202336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30330875-G-A

20202358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30330855-T-A

http://identifiers.org/hco/6/GRCh38#20202416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30330815-C-A

20202470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30330759-T-C

http://identifiers.org/hco/6/GRCh38#20202803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30330464-A-C

20202935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30330354-C-T

20203257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30330203-A-T

20203267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30330193-T-C

http://identifiers.org/hco/6/GRCh38#20203779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30329713-C-A

20204088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30328904-G-A

20204093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30328899-C-T

20204158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30328807-C-T

20204281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30328722-T-C

20207705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30325031-G-A

20207740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30325000-G-A

20207972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30324808-A-T

20208085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30324693-C-G

20208587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30324270-T-C

20208587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30324270-T-G

20210391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30323026-T-C

20210868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30322336-C-T

20211121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30322145-G-T

20211200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30322075-G-A

http://identifiers.org/hco/6/GRCh38#20211563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#30321454-A-C

http://identifiers.org/hco/6/GRCh38#20211578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#30321438-C-A

20211639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30321276-G-A

20211691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30321124-C-G

http://identifiers.org/hco/6/GRCh38#20211973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#30320863-C-A

20211986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30320850-A-G

20211986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30320850-A-T

20212355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21579
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30320585-G-C