96923226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron variant
orthologous variants: 24853873-T-G

96924086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron variant
orthologous variants: 24851455-C-T

96924271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron variant
orthologous variants: 24851285-G-T

96924367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron variant
orthologous variants: 24851191-C-T

96924583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron variant
orthologous variants: 24851058-G-A

http://identifiers.org/hco/6/GRCh38#96924704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24851014-C-A

96924704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 24851014-C-T

96924709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 24851009-G-A

96924848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24850907-C-T

96924968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24850795-G-A

96924968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24850795-G-C

http://identifiers.org/hco/6/GRCh38#96925037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24850725-C-A

96925102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24850648-G-C

96925102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24850648-G-T

96925482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24850292-G-A

96925482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24850292-G-C

96925692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24850092-G-T

96925725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24850058-C-T

96925840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24849969-T-A

96925935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24849879-A-T

96925972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24849843-G-T

96926039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24849759-A-T

96926063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24849735-G-A

96926413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24849397-T-C

96926618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24849203-G-A

96926840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24849098-A-G

96927076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24848770-T-G

96927152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24848697-T-C

96927580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24848296-T-G

96927656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24848260-C-T

96927774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24848188-G-A

96927869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24848115-C-T

96927951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24848023-C-T

96928006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24847980-A-G

96928273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24847609-T-C

http://identifiers.org/hco/6/GRCh38#96928348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24847534-C-A

96928376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24847507-G-C

96928507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24847402-T-C

96928637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24847273-G-A

96928705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24847212-A-G

96928764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24846975-G-A

96928895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24846538-A-T

96929076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24846342-T-A

96929084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24846334-G-T

96929116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24846305-G-C

96929201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24846238-G-A

http://identifiers.org/hco/6/GRCh38#96929455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24846167-C-A

96929638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24845994-A-T

http://identifiers.org/hco/6/GRCh38#96929645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24845987-C-A

http://identifiers.org/hco/6/GRCh38#96929890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24845703-C-A

http://identifiers.org/hco/6/GRCh38#96929942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24845651-A-C

96930063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24845544-C-T

96930288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24845321-A-G

http://identifiers.org/hco/6/GRCh38#96930362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24845252-C-A

96930400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24845214-A-G

96930624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843773-A-G

96930661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843729-C-T

96930707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843708-C-G

96930707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843708-C-T

96930816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843569-G-A

96930914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843433-G-A

96930983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843408-G-A

96931021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843373-G-C

96931096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843298-C-G

96931137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843272-C-T

96931152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843257-A-G

96931197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843214-T-A

96931266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24843124-T-G

96931456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24842892-C-T

96931530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24842835-A-G

96931652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24842724-G-A

96931691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24842688-A-G

96931813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24841940-A-G

96931911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24841841-C-T

96931941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24841810-T-C

96932026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24841730-G-A

96932026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24841730-G-T

96932188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24841589-A-G

http://identifiers.org/hco/6/GRCh38#96932198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24841579-C-A

96932347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24841345-T-A

96932492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24841201-C-G

96932554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24841138-G-T

96934086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24840728-C-G

96934171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24840655-T-C

96934248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24840559-T-C

96934285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24840522-G-T

96934333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24840477-G-A

96934437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839994-C-T

96934469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839969-G-A

96934481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839957-A-T

96934579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839897-G-A

96935119-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839350-T-G

96935224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839220-G-A

96935297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24839150-T-C

96936222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24838250-C-T

96936447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24837872-C-G

96942512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24834941-G-A

96943187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24834419-C-T

96943349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24834280-G-A

96943472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24834172-G-A

96943472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24834172-G-T

96943503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24834139-T-G

http://identifiers.org/hco/6/GRCh38#96943576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24834065-A-C

96943696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24833947-C-G

96943710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24833933-C-T

96943751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24833892-G-T

96943832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24833814-T-G

96943929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24833257-T-C

96944160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24833026-G-A

96944160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24833026-G-T

96944382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24832810-A-G

http://identifiers.org/hco/6/GRCh38#96944553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24832649-C-A

96944679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24832525-A-G

96944701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24832503-G-A

96944741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24832458-G-A

96944899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24832307-T-C

96945358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24830368-C-T

96945406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24830313-A-G

96948465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24830108-T-C

96948465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24830108-T-G

96948470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24830103-G-A

96948477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24830096-C-T

96949087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24829529-G-A

96949589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24829121-T-G

96949640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24829092-C-G

96949718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24828823-T-C

96949766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24828776-C-T

http://identifiers.org/hco/6/GRCh38#96949913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24828297-C-A

96949913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24828297-C-T

96949918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24828292-T-C

96949984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24828226-T-C

96950052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24827952-A-G

96950071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24827929-A-G

96950205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24827802-G-T

96950207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24827800-G-T

96950228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24827779-G-A

96950231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24827776-A-T

96950489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24827552-A-G

96950492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24827549-T-C

http://identifiers.org/hco/6/GRCh38#96950513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24827527-C-A

96950616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24827414-G-A

96950640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24827390-T-A

96950640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24827390-T-C

96950735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24827293-T-C

96951414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24825566-G-A

96951571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24825379-A-T

http://identifiers.org/hco/6/GRCh38#96951794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24825192-A-C

96951852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24825134-G-C

96951852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24825134-G-T

96956407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24814426-G-C

96956544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24814295-T-C

96957147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24813809-G-T

96957247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24813718-T-C

96957592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812951-C-T

96958033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812503-G-C

96958057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812479-A-G

96958114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812442-G-A

http://identifiers.org/hco/6/GRCh38#96958242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24812324-C-A

96958242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812324-C-G

96958242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24812324-C-T

96958790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24804611-G-T

96959002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24804402-G-A

96965328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24802435-T-C

96965728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24802067-A-G

96966167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801651-C-G

96966206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801612-G-A

96966311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801508-A-G

96966826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24801045-A-G

http://identifiers.org/hco/6/GRCh38#96966891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24800991-C-A

96966891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800991-C-G

96966891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800991-C-T

96966895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800987-G-A

96966895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800987-G-T

http://identifiers.org/hco/6/GRCh38#96966917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24800966-A-C

96966917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800966-A-T

96966941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800942-G-T

96966990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24800894-A-G

96967043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24800843-G-A

96967053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24800834-G-C

http://identifiers.org/hco/6/GRCh38#96967089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24800798-C-A

96967089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800798-C-T

96967111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800772-T-G

96967112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800771-G-A

http://identifiers.org/hco/6/GRCh38#96967123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24800716-C-A

96967123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800716-C-T

http://identifiers.org/hco/6/GRCh38#96967124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24800715-C-A

96967131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800708-T-C

http://identifiers.org/hco/6/GRCh38#96967137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24800702-C-A

96967137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800702-C-G

96967137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800702-C-T

96967138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800701-A-G

96967141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800696-G-A

96967141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800696-G-T

96967151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800686-G-A

96967151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800686-G-T

96967156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800617-A-G

http://identifiers.org/hco/6/GRCh38#96967161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24800612-C-A

96967169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800556-G-T

http://identifiers.org/hco/6/GRCh38#96967172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24800553-C-A

http://identifiers.org/hco/6/GRCh38#96967197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24800439-C-A

96967197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800439-C-G

http://identifiers.org/hco/6/GRCh38#96967201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24800435-C-A

96967201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800435-C-G

96967201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800435-C-T

96967356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800265-A-G

96967461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800217-G-A

96967707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800034-A-T

96967717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800024-C-T

96967756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24800000-A-G

96967848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799915-G-A

96967851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799912-G-A

96968008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799765-G-A

http://identifiers.org/hco/6/GRCh38#96968119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24799668-A-C

96968152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799635-G-T

96968197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799594-A-G

96968243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799559-A-G

96968470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799377-T-A

96968816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24799027-T-C

http://identifiers.org/hco/6/GRCh38#96969423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24798299-A-C

96969906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797860-A-G

96969998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797787-C-T

96970038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797744-A-T

96970228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797565-C-T

96970284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797510-C-G

96970314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797484-C-T

96970346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797463-C-G

http://identifiers.org/hco/6/GRCh38#96970353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24797456-C-A

96970424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797379-G-A

96970424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797379-G-C

96970499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797311-C-T

96970590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797220-T-C

96970778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24797045-A-G

96971339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796738-G-C

96971395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796683-A-T

96971464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796617-T-C

96971667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796414-A-T

96972238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24796188-A-G

http://identifiers.org/hco/6/GRCh38#96972423-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24796078-A-C

96972601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24795977-G-T

96972723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24795851-A-G

96972993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24795588-T-A

http://identifiers.org/hco/6/GRCh38#96973002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24795579-A-C

96973267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24795303-C-G

96973670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794719-A-G

96974132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794546-T-C

96974634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794088-T-C

96974668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24794056-C-T

96974934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24793806-C-T

96974988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24793754-G-T

96974994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24793746-C-T

96975187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24793556-T-C

96975607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24793170-A-T

96975847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792939-G-A

96975847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792939-G-T

96975878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792905-A-G

http://identifiers.org/hco/6/GRCh38#96975883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24792900-C-A

96975886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792897-A-T

96975891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792894-G-A

96975891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792894-G-T

http://identifiers.org/hco/6/GRCh38#96975924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24792867-A-C

96975924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792867-A-G

http://identifiers.org/hco/6/GRCh38#96975929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24792862-A-C

96975929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792862-A-G

96976052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24792740-A-G

96976100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24792692-G-A

96976115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24792677-G-A

96976115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24792677-G-T

96976157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24792635-G-A

http://identifiers.org/hco/6/GRCh38#96976241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24792548-A-C

96976241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792548-A-G

http://identifiers.org/hco/6/GRCh38#96976278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24792526-C-A

96976392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792413-C-T

96976451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792364-G-T

96977182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792238-T-A

96977331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24792084-G-A

96977625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24788152-G-A

96994349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787029-A-G

96994349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787029-A-T

96994389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786988-G-A

96994403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786969-T-C

96994463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786901-T-C

http://identifiers.org/hco/6/GRCh38#96994492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24786872-C-A

96994492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786872-C-T

96994524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786840-A-G

96994576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786789-G-A

96994638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786734-A-T

96994673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786699-G-A

96994673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786699-G-C

96994722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786651-C-T

96994741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786632-A-T

96994742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786631-T-A

96994745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786628-T-A

96994756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786617-A-G

96994756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786617-A-T

96994785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786585-A-G

96995118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786285-G-A

96995449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786005-T-G

96995452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786002-A-G

96995575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785917-C-T

96995622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785868-T-C

96995750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785774-T-A

96995945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785597-C-T

96996001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785541-G-A

96996001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785541-G-C

96996094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785402-G-C

96996099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785396-G-C

96996335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785214-A-G

96996403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785157-G-A

96996453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785107-T-C

96996776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784811-G-A

96996861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784725-C-G

96996993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784616-G-A

96997156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784448-A-G

96997160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784444-G-T

96997397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784198-A-G

96997402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24784193-T-C

96997429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781100-T-C

96998237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780734-G-T

96998619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780407-A-G

96998668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780358-T-G

96998682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780344-G-A

96998711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780315-G-A

96998849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780194-G-T

96998855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780188-C-T

97000650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779990-A-G

97000727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779904-A-T

97000850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779784-T-C

97001717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779432-C-G

97001751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779400-G-A

97001763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779388-A-G

97001885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779306-C-T

97001968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779242-T-C

97002125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24779089-G-C

http://identifiers.org/hco/6/GRCh38#97011371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24777535-C-A

http://identifiers.org/hco/6/GRCh38#97011425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24777482-C-A

97011425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24777482-C-T

97011484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24777433-G-T

97011523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24777395-A-G

97011742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24777173-G-A

97011755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24777162-T-C

97013055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24768288-A-G

97013055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24768288-A-T

97013745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24768185-G-T

97017193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24767890-A-T

http://identifiers.org/hco/6/GRCh38#97017195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24767888-C-A

97017420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24767669-T-C

97020319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24767468-A-G

97020360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24767424-A-G

97020603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24767215-C-T

97020608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24767211-C-T

97020740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24767062-C-T

97020742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24767060-A-G

http://identifiers.org/hco/6/GRCh38#97020947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24766869-C-A

97020989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24766827-A-G

97024216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24765718-A-G

97024519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24765437-G-T

97025164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24764819-T-C

97025167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24764816-G-A

http://identifiers.org/hco/6/GRCh38#97025400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24764579-C-A

97025535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24764445-C-T

97027301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24756314-T-C

97027308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24756307-C-T

97027500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24756112-G-A

97027500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24756112-G-C

97027569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24756060-T-C

97027646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24755986-T-C

97027664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24755960-A-G

97027920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24755762-A-G

http://identifiers.org/hco/6/GRCh38#97027990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24755698-A-C

97028109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24755593-C-G

97028126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24755579-G-A

97028147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24755557-A-G

97028147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24755557-A-T

97028966-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24754750-G-C

97029184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24754558-G-A

97029251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24754491-C-T

97029334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24754417-A-G

97029343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24754408-A-G

97029784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753542-G-T

97029890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753407-C-T

97030041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753250-T-A

97030140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753183-C-T

97030156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753166-C-G

97030268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753049-T-C

97030310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24753008-G-A

97030386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24752928-G-A

97030558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24752758-C-T

97030806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24752532-A-G

97030806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24752532-A-T

http://identifiers.org/hco/6/GRCh38#97041353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24744109-C-A

http://identifiers.org/hco/6/GRCh38#97041354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24744108-A-C

97041354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24744108-A-G

97041383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24744079-T-G

http://identifiers.org/hco/6/GRCh38#97041452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24744010-C-A

http://identifiers.org/hco/6/GRCh38#97041640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24743815-C-A

http://identifiers.org/hco/6/GRCh38#97041731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24743726-C-A

97041866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24743594-C-T

97041919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24743545-C-T

97041920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24743544-G-A

97041920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24743544-G-C

97045084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24739873-T-C

97045106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24739851-C-T

97045147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24739814-G-A

97045173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24739790-A-G

97045373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24739591-C-T

97046180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24738413-C-T

97046233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24738356-A-G

97046491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24737978-G-A

http://identifiers.org/hco/6/GRCh38#97046518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24737952-A-C

97046518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24737952-A-G

97046713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24737618-A-T

97046756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24737575-C-T

97046758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24737573-T-G

97047041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24737276-G-A

97047098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24737223-A-G

97047457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736923-T-G

97047581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736807-T-C

97047645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736741-C-T

97048040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736398-A-G

97048198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736249-C-T

97048343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24736116-A-G

97048489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24735976-A-G

97048718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24735570-A-G

97049683-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24734571-A-T

97049783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24734468-G-T

97049792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24734459-T-C

97049808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24734449-C-T

97049836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24734422-C-G

97050023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24734069-T-C

97050106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24733986-T-C

97050135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24733957-A-G

97052085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722673-C-T

97052088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722670-A-G

97052122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722630-G-A

http://identifiers.org/hco/6/GRCh38#97052127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24722625-A-C

97052171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722587-G-C

97052204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722557-G-A

97052352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722434-A-G

97052352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722434-A-T

97052776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24722074-G-A

97053699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24721199-G-A

97054042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24720980-G-T

97054101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24720923-G-A

97054121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24720887-T-C

97054188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24720766-T-C

97054280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24720685-G-A

97054379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24720587-A-G

97054471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24720494-G-A

97059573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24714586-A-T

97059579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24714580-C-T

97059896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24714306-T-C

97059979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24714238-C-G

97059979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24714238-C-T

97060113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24714124-A-G

97060133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24714103-G-A

97060133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24714103-G-C

97060156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24714082-A-G

97060165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24714073-A-G

97060171-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24714068-T-A

97060314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24713938-A-G

97060316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24713936-A-G

97060500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24713811-T-C

97060529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24713786-C-T

97060536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24713781-T-C

97060573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24713744-T-C

97060638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24713668-T-A

97060687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24713620-T-C

http://identifiers.org/hco/6/GRCh38#97060779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24713535-C-A

97060937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24712923-G-A

97061073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24712831-C-T

97061186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24712722-A-G

97061308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24712615-G-T

97061467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24712495-T-C

97061547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24712416-G-C

97061662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24712311-A-G

http://identifiers.org/hco/6/GRCh38#97061703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24712256-C-A

97061785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24712159-T-A

97061907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24712039-G-A

97061907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24712039-G-C

97062028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24711919-T-C

http://identifiers.org/hco/6/GRCh38#97062138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24711809-A-C

97062175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24711772-T-C

97062357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24711589-A-G

97062402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24711544-T-C

97062434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24711513-G-A

97062505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 24711444-T-C

97062506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24711443-T-C

97062522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24711427-T-C

97062546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24711403-A-G

97062594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24711344-A-G

97062687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24711247-T-C

97062738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24711203-C-T

97063771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24709893-G-A

97064005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24709696-C-T

97064127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24709594-T-C

http://identifiers.org/hco/6/GRCh38#97064303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24709369-C-A

97064546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24709135-T-C

97064549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24709132-T-C

97064598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24709080-T-C

http://identifiers.org/hco/6/GRCh38#97064800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24708895-C-A

97064800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708895-C-T

97064815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708875-A-G

97064833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708848-G-C

97064833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708848-G-T

97064844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708838-G-A

97064844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708838-G-T

97064864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24708764-A-G

97064902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708727-C-T

97064926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708705-A-G

97065169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708432-G-A

97065169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708432-G-T

97065245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708351-A-G

97065283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708315-C-G

97065334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24708267-A-G

97065603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24707563-C-T

97065746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24707413-T-A

97066032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24707085-G-A

97066066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24707051-C-T

97066304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24706816-G-A

97066408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24706719-C-T

97066414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24706713-A-G

97066490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24706637-C-T

97066511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24706617-A-G

97066618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24706517-G-A

97066618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24706517-G-T

97066666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24706476-A-T

97067640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699555-G-T

97067666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699519-G-A

97067704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699481-A-G

97067938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699283-C-T

97067985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699235-T-G

97068159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699108-C-T

97068166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699104-C-G

97068166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699104-C-T

97068210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24699067-T-C

97068499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24698796-A-T

97068980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24698315-C-T

97069178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24698125-G-T

97069197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24698106-G-A

97069197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24698106-G-C

97069204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24698095-G-A

97069250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24698046-T-C

97069350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697946-A-T

97069459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697790-C-T

97069541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697710-A-G

97069546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697705-T-A

97069645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697606-C-G

97069645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697606-C-T

97069657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697594-C-T

97069818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697432-T-G

97069910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697339-T-A

97069910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697339-T-C

97069966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697283-A-T

97070004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697253-A-T

97070046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697214-C-T

97070246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24697012-G-A

97070317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24696949-T-C

97070519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24696748-G-A

97070615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24696654-G-A

97070788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24696471-G-A

97070871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24696393-G-A

97070871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24696393-G-T

97071809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24696103-T-G

97071842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24696070-C-T

97071944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24695978-A-G

97072322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24695636-C-T

97072443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24695535-A-G

97075023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24694801-C-G

97075023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24694801-C-T

97076136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24693712-T-C

97076210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24693260-G-A

97076239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24693231-A-T

http://identifiers.org/hco/6/GRCh38#97076330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24693152-C-A

97076450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24693052-G-A

97076546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24692970-T-C

97077614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24692575-C-T

97077633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24692556-G-A

97077810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24692417-C-T

97078845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24691414-G-A

http://identifiers.org/hco/6/GRCh38#97078918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24691345-A-C

http://identifiers.org/hco/6/GRCh38#97078920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24691343-C-A

97078920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24691343-C-T

97079097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24691161-A-G

97079375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24690899-C-G

97079619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24690665-G-C

http://identifiers.org/hco/6/GRCh38#97079634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24690650-C-A

97079648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24690636-A-G

97080046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24690245-G-C

97080209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24690058-A-G

97082175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24688537-T-C

97082201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24688510-C-T

97082626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24688248-T-A

97082634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24688240-T-A

97082640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24688229-G-C

97082684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24688197-G-T

97082784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24688090-G-A

97082860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24688011-G-A

http://identifiers.org/hco/6/GRCh38#97083965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24686785-C-A

97084056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24686689-A-G

97084058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24686687-G-T

97084262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24683824-C-G

97084726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24683408-C-T

97084913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24682450-G-A

97084924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24682439-T-G

97084966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24682426-G-A

97084999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24682389-T-C

97084999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24682389-T-G

http://identifiers.org/hco/6/GRCh38#97085018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24682372-C-A

97085018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24682372-C-G

http://identifiers.org/hco/6/GRCh38#97085019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24682371-C-A

97085019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24682371-C-T

97085061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24682330-T-C

97085354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24682040-T-G

97085388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24682016-G-A

97085389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24682015-T-G

http://identifiers.org/hco/6/GRCh38#97085403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24682001-A-C

97085465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24681944-T-C

97085475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24681934-T-C

97085479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24681930-T-A

97085741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24681704-T-C

97085753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24681691-A-G

97085936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24680264-A-G

97085945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24680256-T-C

97085965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24680236-A-G

97086034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24680167-G-A

97086067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24680140-A-G

97086072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24680135-A-G

97086191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24680029-A-T

97086341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24679901-T-C

97086725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24679579-T-C

97086769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24679535-T-A

97086814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24679491-G-A

http://identifiers.org/hco/6/GRCh38#97086927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24679385-C-A

97087056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24679256-C-T

97087873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24678464-C-T

97088218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24677846-T-A

http://identifiers.org/hco/6/GRCh38#97088386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24677677-C-A

97088507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24677540-G-A

97088599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24677487-C-G

http://identifiers.org/hco/6/GRCh38#97088668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24677421-A-C

97088668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24677421-A-G

97088943-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24677061-T-A

97088943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24677061-T-C

97089972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24676317-T-C

97090057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24676261-G-A

97090151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24676160-T-A

97090218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24676097-A-G

97090612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24675730-C-G

97090659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24675687-A-G

97090665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24675681-C-T

97090679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24675668-A-G

97090878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24675488-G-A

97090934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24675444-G-T

97091423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24675175-T-A

97091448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24675150-C-G

http://identifiers.org/hco/6/GRCh38#97091698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24674983-C-A

97092481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674564-A-G

97092486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674560-A-G

97092594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674484-C-G

97092661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674421-T-C

97092675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674407-G-C

97092699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674385-C-T

97092751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674335-T-C

97092928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674158-T-C

97092984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674084-G-A

97093002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24674066-G-T

97093246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673825-C-T

97093489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673577-T-C

http://identifiers.org/hco/6/GRCh38#97093664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24673413-C-A

97093664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673413-C-T

97093739-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673334-T-A

97093756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673317-C-T

97093858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673239-A-G

97093881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24673217-A-G

97094125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672983-T-C

97094199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672922-A-G

97094263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672858-T-C

97094297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672824-C-G

http://identifiers.org/hco/6/GRCh38#97094343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24672779-C-A

http://identifiers.org/hco/6/GRCh38#97094464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24672606-C-A

97094476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672564-C-T

97094577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672457-C-G

97094675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672359-A-G

97094741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672289-A-G

97094816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672218-C-G

97094853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24672181-G-T

http://identifiers.org/hco/6/GRCh38#97095110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24671936-A-C

97095322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24671730-A-T

97095479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24671587-G-A

97095541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24671526-T-A

97095559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24671508-A-G

97095777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24671316-G-T

http://identifiers.org/hco/6/GRCh38#97096011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24671112-A-C

97096156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24670954-A-G

97096522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24670535-A-G

http://identifiers.org/hco/6/GRCh38#97097800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24669276-A-C

97097805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24669271-G-A

http://identifiers.org/hco/6/GRCh38#97097936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24669142-A-C

97098566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24666649-T-C

http://identifiers.org/hco/6/GRCh38#97098689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24666532-A-C

97098689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24666532-A-G

97098705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24666517-T-C

97099118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24665984-A-G

97099120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24665982-G-A

97099146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24665956-C-T

97099354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24665496-T-A

97099355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24665495-C-T

97099378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24665472-G-C

97099474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24665374-G-C

http://identifiers.org/hco/6/GRCh38#97099497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24665348-A-C

97099578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24665268-C-G

97099612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24665235-G-A

97100633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24664595-C-T

97100772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24664463-G-A

97100772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24664463-G-C

http://identifiers.org/hco/6/GRCh38#97100777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24664458-C-A

97100777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24664458-C-T

97100778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24664457-T-G

97100790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24664450-C-T

http://identifiers.org/hco/6/GRCh38#97101507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24663839-A-C

97101628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24663733-A-G

97101663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24663699-A-T

97101757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24663609-G-A

97101887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24663484-C-T

http://identifiers.org/hco/6/GRCh38#97101989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24663308-C-A

97102050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24663245-C-G

97102055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24663240-A-G

97102117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24663149-A-G

97102372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24662853-A-G

97102463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24662787-A-G

97102472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24662778-A-G

97102736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24662513-G-C

97104635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24659509-G-A

97105307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24658720-T-C

97105458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 24658572-G-A

97105634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24658403-T-A

http://identifiers.org/hco/6/GRCh38#97105655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24658388-C-A

97105655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24658388-C-T

97105724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24658330-A-G

97105747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24658307-A-G

97105845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24658215-C-T

97106802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24654939-A-G

97107358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24654690-T-C

97107630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24654412-C-T

97107681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24654362-C-T

97107909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24654134-G-T

97108034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24654009-T-C

97108039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24654004-G-T

97108086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24653959-T-A

97108386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24653588-A-G

97108428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24653547-A-G

97108535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24653454-G-A

97108535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24653454-G-T

97109458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24652197-C-T

97109564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24652144-A-G

97109795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24651939-G-A

97109946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24651804-G-T

97110048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24651699-A-G

97110048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24651699-A-T

97110049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24651698-T-C

97110083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24651663-G-T

97110084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24651662-G-A

97110084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24651662-G-T

97110336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24651484-G-A

97110506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24651368-G-C

97110557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24651314-G-A

97113146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24650847-G-A

97113184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24650807-T-C

97113226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24650762-A-T

97113399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24650599-C-T

97113594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24650410-T-C

97113662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24650351-T-C

97113668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24650345-G-A

http://identifiers.org/hco/6/GRCh38#97113709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24650310-C-A

97114092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 24649955-G-A

97114197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 24649850-C-T

97114347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 24649700-G-A

97114516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24649531-C-T

97114529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 24649516-G-T

97114544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 24649501-C-T

http://identifiers.org/hco/6/GRCh38#97114655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24649391-C-A

97114655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24649391-C-T

http://identifiers.org/hco/6/GRCh38#97114708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24649335-C-A

97114708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24649335-C-G

97114708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24649335-C-T

http://identifiers.org/hco/6/GRCh38#97114759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24649284-A-C

97114812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24649223-T-C

97115385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24648928-C-T

97115544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24648826-A-G

97115937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24648516-C-T

97115981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24648477-T-C

97116727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24647734-G-A

97116727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24647734-G-T

97116774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24647692-A-G

97116999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24647473-T-C

97117034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24647438-A-G

97117062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24647410-G-A

97117179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24647297-T-G

97117235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24647240-A-G

97117255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24647217-T-A

97117255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24647217-T-G

97117337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24647136-G-T

97117415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24647056-G-C

97117566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24646915-G-A

http://identifiers.org/hco/6/GRCh38#97117644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24646834-C-A

97117662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24646816-A-G

97117852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24646636-T-C

97118061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24646425-G-A

97118080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24646389-A-G

97118098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24646371-A-G

97118660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24643415-T-A

97118691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24643384-G-A

97118700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24643375-G-C

97118707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24643368-G-A

97118734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24643339-G-C

97118836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24643240-A-G

http://identifiers.org/hco/6/GRCh38#97119117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24643007-A-C

97119283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24642397-T-C

97119414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24642285-T-C

97119527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24642075-A-G

97119703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24641923-A-T

97119704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24641922-T-G

97119747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24641880-T-A

97119972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24641672-A-G

97119981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24641663-G-T

97120208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24641451-C-T

97120277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24641347-A-T

97120425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24641198-T-C

97120534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24641116-T-G

97120535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24641115-G-C

97120561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24641089-T-C

97120563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24641087-A-G

97120758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24640964-G-A

97120758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24640964-G-T

http://identifiers.org/hco/6/GRCh38#97120779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24640944-C-A

97120812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24640907-A-G

97120902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24640799-T-C

97120953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24640722-T-C

97120986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24640690-A-G

97121078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24640600-A-G

97121081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24640597-G-C

http://identifiers.org/hco/6/GRCh38#97121299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24640370-A-C

97121299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24640370-A-G

97121337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24640333-G-T

97121361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24640309-C-T

97121938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24639782-A-G

97121956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24639762-G-A

97122721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24637417-G-A

97122779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24637363-A-G

97122893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24637275-C-T

http://identifiers.org/hco/6/GRCh38#97122909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24637255-C-A

97123033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24637151-T-C

97123132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24637006-A-T

97123216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24636843-C-T

97123354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24636624-G-T

97124098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24635882-A-G

97124508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24635459-T-C

97124566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24635424-A-G

97124745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24635263-G-A

97124855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24635153-G-T

97125000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24635013-T-C

97125256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24634741-G-C

97125311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24634680-G-A

97125554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24634482-T-C

97125689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24634381-G-A

97125689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24634381-G-T

97125980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24634200-A-G

97126063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24634131-G-A

97126063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24634131-G-T

97126134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24634061-G-A

http://identifiers.org/hco/6/GRCh38#97126136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24634059-C-A

97126136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24634059-C-T

http://identifiers.org/hco/6/GRCh38#97126153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24634042-C-A

97126153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24634042-C-G

97126344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24633974-G-T

97126531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24633471-G-T

97126564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24633447-G-A

97126624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24633384-C-T

97126803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24633228-G-A

http://identifiers.org/hco/6/GRCh38#97127300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24632804-A-C

97127330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24632773-T-A

97127475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24632628-T-C

97127475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24632628-T-G

97127525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24632579-A-G

97127525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24632579-A-T

97127526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24632578-T-A

97127526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24632578-T-C

97127526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24632578-T-G

97127590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24632528-A-T

97127597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24632517-T-A

http://identifiers.org/hco/6/GRCh38#97127736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24632403-C-A

97127736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24632403-C-T

97127775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24632365-T-C

97127910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24632242-A-G

97128071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24632110-C-T

97128388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24631744-C-T

97128608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24631523-T-G

97128963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24631177-C-G

97129229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24630638-G-A

97129484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24630370-A-G

97129490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24630364-G-T

http://identifiers.org/hco/6/GRCh38#97130430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24629645-A-C

97130430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24629645-A-G

97130606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24629484-T-A

97130606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24629484-T-C

97130618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24629474-T-C

97130972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24629096-A-G

http://identifiers.org/hco/6/GRCh38#97130997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24628829-C-A

97130997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24628829-C-T

97131019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24628807-T-A

97131021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24628805-T-G

97131088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24628737-T-C

97131089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24628736-G-A

97131164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24628675-C-T

97131197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24628640-T-C

http://identifiers.org/hco/6/GRCh38#97131217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24628620-A-C

97131451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24628198-G-A

97131616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24628034-C-T

97132104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24627554-C-T

97132290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24627366-G-A

97132396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24627242-C-G

97132442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24627199-T-G

97132506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24627134-G-C

http://identifiers.org/hco/6/GRCh38#97132525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24627115-C-A

97132525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24627115-C-T

97132790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626852-A-G

http://identifiers.org/hco/6/GRCh38#97132856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24626789-C-A

97132856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626789-C-T

http://identifiers.org/hco/6/GRCh38#97133037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24626623-A-C

97133064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626596-C-T

97133176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626492-C-T

97133194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626474-G-A

97133194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626474-G-C

97133342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626340-A-T

97133348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626334-C-G

97133393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626301-G-A

97133398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24626296-C-T

97133867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24625657-T-G

http://identifiers.org/hco/6/GRCh38#97134120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24625417-C-A

97134730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24624699-A-G

97134893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24624544-T-A

97135163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24624107-T-C

97135315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24623990-T-C

97135703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24623352-G-A

97135791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24622515-T-C

97135910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24622388-A-G

97135922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24622374-T-A

97136307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24622030-A-G

97136421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24621917-T-A

97136421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24621917-T-C

97136709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24621653-C-T

97136962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24621448-T-C

97136982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24621421-G-A

97136982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24621421-G-C

97136982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24621421-G-T

97136998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24621405-G-A

97137077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24621334-A-G

97139059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24617587-A-G

97139247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24617418-C-T

http://identifiers.org/hco/6/GRCh38#97139318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24617351-C-A

97139338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24617331-G-A

97139338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24617331-G-T

97139368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24617308-T-A

97139368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24617308-T-C

97139414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24617254-A-G

97139611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24617054-G-A

97139611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24617054-G-T

http://identifiers.org/hco/6/GRCh38#97139615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24617050-A-C

http://identifiers.org/hco/6/GRCh38#97139627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24617043-C-A

97139627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24617043-C-T

97139655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24617021-T-C

97139655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24617021-T-G

97139660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24617016-T-A

97139668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24617008-T-C

97139668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24617008-T-G

97139719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24616964-A-G

97139720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24616963-A-G

97139755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24616932-G-T

http://identifiers.org/hco/6/GRCh38#97139763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24616924-A-C

97139796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24616890-A-G

97139841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24616868-T-C

http://identifiers.org/hco/6/GRCh38#97140013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24616710-A-C

97140220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24616524-T-C

97140231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24616513-A-G

97140309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24616461-A-G

http://identifiers.org/hco/6/GRCh38#97140316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21221
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24616454-C-A