99875758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43835416-G-T

http://identifiers.org/hco/10/GRCh38#99875763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43835421-A-C

99875769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43835427-G-A

99875769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43835427-G-T

http://identifiers.org/hco/10/GRCh38#99875882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43835510-C-A

99876028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43835668-C-T

99876040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43835680-A-G

http://identifiers.org/hco/10/GRCh38#99876060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43835697-C-A

99876121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43835754-C-T

99876137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43835757-G-C

99876137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43835757-G-T

99876162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43835783-C-T

99876178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43835799-T-C

99876186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43835813-T-C

99876252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43835879-C-T

99876266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43835884-A-G

99876439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43835945-A-G

99876577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43836022-T-C

http://identifiers.org/hco/10/GRCh38#99876591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43836036-C-A

99876809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43836219-G-T

99876834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43836242-G-A

99876834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43836242-G-T

http://identifiers.org/hco/10/GRCh38#99876863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43836267-C-A

99876953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43836355-A-G

99877018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43836413-G-A

99877018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43836413-G-T

99877027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43836419-T-C

99877028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43836420-G-A

99877105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43836490-G-A

99877105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43836490-G-T

99877146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43836528-T-G

99877147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43836529-G-C

99877147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 3 prime UTR variant
orthologous variants: 43836529-G-T

99879523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43837945-C-T

99879852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense variant
orthologous variants: 43838256-T-C

99879914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense variant
orthologous variants: 43838318-C-T

99879926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense variant
orthologous variants: 43838330-G-A

99879957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense variant
orthologous variants: 43838361-T-G

99880248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense variant
orthologous variants: 43838652-A-G

99880261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: 43838665-C-T

99880342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: 43838746-G-A

http://identifiers.org/hco/10/GRCh38#99884117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43840769-A-C

99884153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: 43840805-G-A

99884239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43840896-T-C

99884258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43840911-C-T

99884950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43841922-T-C

99884951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43841923-G-A

99884999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43841984-C-T

99885184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43842178-C-T

http://identifiers.org/hco/10/GRCh38#99885955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43842960-C-A

99885966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43842971-G-A

99885966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43842971-G-T

99885990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43842996-A-G

99886071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43843071-G-A

http://identifiers.org/hco/10/GRCh38#99886152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43843131-A-C

99886165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43843144-T-C

99886165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43843144-T-G

http://identifiers.org/hco/10/GRCh38#99886265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43843205-A-C

99886266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43843206-G-A

99886266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43843206-G-T

99886273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43843213-A-T

99886339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: 43843275-A-G

99886456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43843392-C-G

99886548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43843484-G-A

99886604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43843540-G-C

99886643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43843579-G-A

99886643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43843579-G-C

99888722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43844822-G-T

99888727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43844827-G-A

99888727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43844827-G-T

http://identifiers.org/hco/10/GRCh38#99888766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43844863-C-A

99888766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43844863-C-G

http://identifiers.org/hco/10/GRCh38#99888815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43844931-A-C

99889068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43845175-T-C

99889076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43845183-G-A

99889076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43845183-G-T

http://identifiers.org/hco/10/GRCh38#99889165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43845265-A-C

99894783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43854880-A-G

http://identifiers.org/hco/10/GRCh38#99894799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43854896-C-A

99894799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43854896-C-T

http://identifiers.org/hco/10/GRCh38#99894803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43854900-C-A

99894803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43854900-C-T

99894823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43854920-T-A

99894823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43854920-T-C

http://identifiers.org/hco/10/GRCh38#99894898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43854989-C-A

99894930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855012-T-A

99894930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855012-T-G

99894933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855015-T-C

99894958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: 43855040-G-A

99894970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: 43855052-C-T

99894978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: stop gained
orthologous variants: 43855060-G-A

99895152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855169-G-A

99895152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855169-G-T

99895156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855173-T-C

99895156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855173-T-G

99895213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855189-G-A

99895213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855189-G-T

99895237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855216-C-T

99895254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855227-A-G

http://identifiers.org/hco/10/GRCh38#99895699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43855415-C-A

99895699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855415-C-G

http://identifiers.org/hco/10/GRCh38#99895759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43855463-A-C

99895760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855464-C-T

99895784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855487-C-T

99895896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855588-C-T

99896056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855745-G-C

99896069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855758-T-C

http://identifiers.org/hco/10/GRCh38#99896139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43855842-C-A

http://identifiers.org/hco/10/GRCh38#99896226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43855927-C-A

99896226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43855927-C-G

http://identifiers.org/hco/10/GRCh38#99896270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43855969-A-C

99896466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856208-T-A

99896466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856208-T-C

99896466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856208-T-G

99896474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856216-C-G

99896482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856224-A-G

99896485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856227-T-C

99896531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856277-A-G

99896540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856287-G-A

99896540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856287-G-T

99896571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856314-A-G

99896966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856651-C-T

99897033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856712-A-G

99897047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856726-C-T

99897233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856883-G-A

99897289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856946-G-A

99897326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856986-G-T

99897330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43856990-T-A

http://identifiers.org/hco/10/GRCh38#99897983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43857165-C-A

99897983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857165-C-T

99897985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857167-A-G

99897997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857178-G-A

99897997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857178-G-T

99898013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857194-G-A

99898013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857194-G-C

99898013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857194-G-T

http://identifiers.org/hco/10/GRCh38#99898047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43857205-A-C

99898050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857208-G-A

99898071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857229-T-A

http://identifiers.org/hco/10/GRCh38#99898138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43857296-C-A

99898138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: 43857296-C-G

99898138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: 43857296-C-T

99898139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense variant
orthologous variants: 43857297-G-A

99898150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: 43857308-A-G

99898172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense variant
orthologous variants: 43857330-G-A

99898216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: 43857374-C-T

http://identifiers.org/hco/10/GRCh38#99898475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43857760-A-C

99898475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857760-A-G

99898475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857760-A-T

99898669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857951-C-T

99898690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857972-G-A

99898690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857972-G-C

99898690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43857972-G-T

99898735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 43858020-G-A

http://identifiers.org/hco/10/GRCh38#99898776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43858060-C-A

99898776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43858060-C-T

http://identifiers.org/hco/10/GRCh38#99899860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43858550-C-A

99899860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43858550-C-T

99899972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: 43858654-G-A

99900092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43858774-T-C

99900093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43858775-G-A

99900166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43858843-A-G

99900166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43858843-A-T

http://identifiers.org/hco/10/GRCh38#99900167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43858844-C-A

http://identifiers.org/hco/10/GRCh38#99900192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43858866-C-A

99900240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43858912-A-G

99900273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43858943-T-C

99901558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43859696-T-C

99901567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43859705-T-C

99901593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43859731-T-C

99904487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43860006-C-T

99904499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43860017-G-A

99904567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43860109-T-C

99904568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43860110-G-A

99904576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43860118-G-A

99904809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43860350-G-A

99907811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43862451-C-T

99907984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43862586-G-A

99908097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 43862699-G-A

99908097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 43862699-G-T

99908122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43862724-T-C

http://identifiers.org/hco/10/GRCh38#99908167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43862767-C-A

99908167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43862767-C-T

http://identifiers.org/hco/10/GRCh38#99908245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43862819-C-A

99908245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43862819-C-T

99908431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43862962-C-T

99908570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43863008-T-C

99908662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43863059-G-A

99908667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43863065-G-A

99908972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense variant
orthologous variants: 43863285-A-G

99909067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: 43863380-C-T

99909109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: 43863422-C-T

http://identifiers.org/hco/10/GRCh38#99909110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43863423-A-C

99909115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: synonymous variant
orthologous variants: 43863428-T-G

99909140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense variant
orthologous variants: 43863453-G-A

99909140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense variant
orthologous variants: 43863453-G-T

99909159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43863472-A-G

99909234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43863541-A-G

99909254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43863561-T-A

99909254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43863561-T-C

99909254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43863561-T-G

http://identifiers.org/hco/10/GRCh38#99909264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43863571-C-A

99909284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43863584-G-A

99909284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43863584-G-T

99909965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43864325-C-T

http://identifiers.org/hco/10/GRCh38#99910022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43864371-A-C

http://identifiers.org/hco/10/GRCh38#99911862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43866088-C-A

99911962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43866381-A-G

99912054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43866468-C-T

99912097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43866511-T-A

http://identifiers.org/hco/10/GRCh38#99912106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43866519-A-C

99912116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43866529-T-G

99912213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43866618-T-C

99912264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43866676-C-T

99912347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43866762-G-C

99912410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43866820-T-C

99912885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43867138-C-G

99913253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43867414-C-G

99913253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43867414-C-T

99913562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43867729-G-A

99913698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43867859-T-C

99913701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43867862-A-G

99913711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43867872-G-C

99913720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43867881-C-T

http://identifiers.org/hco/10/GRCh38#99913865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43867998-C-A

99913865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43867998-C-T

99913878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43868011-G-T

99913933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43868039-T-C

http://identifiers.org/hco/10/GRCh38#99913963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43868062-C-A

99913963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 43868062-C-T

99914010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 43868099-G-A

99914010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 43868099-G-C

http://identifiers.org/hco/10/GRCh38#99914046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43868134-C-A

99914046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 43868134-C-T

99914053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 43868142-A-G

99914068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 43868157-G-A

99914068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 43868157-G-T

99914072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 43868161-G-A

99914072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 43868161-G-T

99914099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43868187-A-G

99914133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43868220-A-G

99914226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43868295-T-C

99914304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43868349-C-T

http://identifiers.org/hco/10/GRCh38#99914536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43868511-C-A

99914536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43868511-C-G

99914739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43868695-C-T

99915821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43869288-A-T

99915874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43869342-G-A

99915874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43869342-G-C

99915943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43869388-T-C

99915975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43869402-C-T

99916005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43869434-C-T

99917504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43871128-T-C

99917504-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43871128-T-G

99917548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43871180-A-G

99918143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43871474-T-C

99918174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43871505-G-C

99918840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43871962-C-T

99918901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43872003-T-G

http://identifiers.org/hco/10/GRCh38#99918983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43872080-A-C

99925944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43874605-T-C

99925965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43874626-C-T

99926112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43874764-G-A

99926373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43874906-C-G

99926754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43875213-T-A

99926754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43875213-T-C

http://identifiers.org/hco/10/GRCh38#99926886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43875250-C-A

http://identifiers.org/hco/10/GRCh38#99926895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43875254-C-A

99926958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43875304-A-G

99927006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43875353-C-T

99927047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43875394-A-G

http://identifiers.org/hco/10/GRCh38#99927049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43875396-C-A

99927049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43875396-C-T

http://identifiers.org/hco/10/GRCh38#99927107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43875463-C-A

99927107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43875463-C-T

99927146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43875500-A-G

99927146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43875500-A-T

99927278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43875616-A-G

99927301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 43875634-T-G

99927306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 43875639-G-A

99927306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 43875639-G-T

99927329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43875662-G-A

99927341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43875682-T-A

99927394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43875786-A-G

http://identifiers.org/hco/10/GRCh38#99927575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43876103-A-C

99927588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43876116-A-G

99927990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43876487-T-C

99928167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43876670-T-C

99928200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43876705-G-T

http://identifiers.org/hco/10/GRCh38#99928329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43876947-C-A

http://identifiers.org/hco/10/GRCh38#99929185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43877357-C-A

99929280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43877450-G-A

99929337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43877504-A-G

99929361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43877523-G-A

99929378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43877540-T-C

99929427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43877596-T-C

99929429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43877598-G-A

99929429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43877598-G-C

99929522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43877664-G-A

99929522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43877664-G-T

99929594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43877735-G-A

99929594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43877735-G-C

99929663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43877804-T-C

99929663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43877804-T-G

99929711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43877852-T-C

99929750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43877888-T-C

99929779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43877917-G-T

99929796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43877934-C-T

99929885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43878020-A-G

99929939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43878068-A-G

99929979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43878111-T-A

99929979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43878111-T-G

99930078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43878213-T-C

99930122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43878257-A-G

99930269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43878404-A-T

99930279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43878414-C-G

99930279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43878414-C-T

http://identifiers.org/hco/10/GRCh38#99930314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43878449-C-A

99930402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43878537-G-A

99930402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43878537-G-T

http://identifiers.org/hco/10/GRCh38#99930423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43878558-C-A

99930423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43878558-C-G

99930439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43878574-C-T

99930563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43878698-T-C

99930614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43878749-G-A

99930653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43878788-T-C

99930677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43878812-C-T

http://identifiers.org/hco/10/GRCh38#99930793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43878925-C-A

99931093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43879225-G-A

99931093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43879225-G-T

99931123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43879255-G-A

http://identifiers.org/hco/10/GRCh38#99931264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43879396-C-A

99931296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43879402-G-C

99931394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43879491-A-G

99931402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43879499-C-G

99931402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43879499-C-T

99931446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43879538-C-G

99931446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43879538-C-T

http://identifiers.org/hco/10/GRCh38#99931598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43879665-A-C

99931611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43879678-G-C

99931665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43879735-G-A

99931859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43879896-G-C

99932280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43880352-C-T

http://identifiers.org/hco/10/GRCh38#99932335-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43880398-A-C

99932335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43880398-A-G

99932336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43880399-T-G

99933442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893861-C-G

99933442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893861-C-T

http://identifiers.org/hco/10/GRCh38#99933450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43893853-A-C

http://identifiers.org/hco/10/GRCh38#99933472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43893835-C-A

99933507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893801-A-G

99933688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893637-A-G

99934064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893578-A-G

99934105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893536-A-G

http://identifiers.org/hco/10/GRCh38#99934106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43893535-C-A

99934106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893535-C-T

99934168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893501-T-C

99934199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893463-G-A

99934202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893460-G-A

99934349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893317-T-C

99934451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43893083-T-C

99934565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43892974-T-A

99934618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43892820-T-A

99934650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43892789-A-T

99934683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43892762-T-G

99936118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43891959-G-T

99938055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43882424-T-G

99942967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43883624-A-G

99943011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43883648-G-A

99943059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43883677-C-T

99943060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43883678-G-A

99943078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43883694-C-T

99943095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43883707-G-A

99943142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43883760-G-A

99943153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43883771-C-T

99943412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43884042-T-G

99943426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43884056-C-T

99943517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43884100-C-T

99943959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43884421-T-C

99944109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43885066-G-C

99944125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43885084-C-G

http://identifiers.org/hco/10/GRCh38#99944177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43885134-A-C

99944188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43885143-G-A

99944252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43885205-A-G

99944262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43885215-A-T

99944387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43885395-T-C

99944415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43885423-C-T

99944534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43885694-C-G

99944549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43885709-C-T

99944601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43885759-C-T

99944658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43885795-T-C

http://identifiers.org/hco/10/GRCh38#99944872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43885984-C-A

99944872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43885984-C-G

99944889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43885998-G-C

99945339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43886659-T-C

99945492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43886791-T-C

99953120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

99953194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43888964-G-A

99953194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43888964-G-T

99954453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43889428-T-C

99954453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43889428-T-G

99955221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43889516-T-C

99955417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43889712-T-C

99955433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43889728-T-C

99955488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43889783-G-A

99955554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43889849-T-G

99955654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43889949-G-A

99955710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43890005-A-G

99955731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43890026-G-A

99955747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43890042-T-C

99955758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43890053-T-G

99955850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43890142-C-T

http://identifiers.org/hco/10/GRCh38#99955879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43890171-A-C

99955923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43890215-G-C

99955924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43890216-A-G

99955927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43890219-G-C

99955927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43890219-G-T

99955967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43890274-C-G

99955967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43890274-C-T

99955992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43890293-T-C

99956013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43890314-T-C

99956013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43890314-T-G

99956060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43890361-G-C

99956073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43890374-C-T

99956091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43890392-G-T

99956130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43890431-G-A

99956130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43890431-G-C

99956131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43890432-G-A

99956131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43890432-G-C

http://identifiers.org/hco/10/GRCh38#99956202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43890503-C-A

99956202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43890503-C-T

99956222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43890523-C-T

99956284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43890585-G-A

99956530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43890819-C-T

99956766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43891055-C-T

99956805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43891094-A-G

99956825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43891114-G-C

99956825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43891114-G-T

99956870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43891159-A-G

99957022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43891311-C-T

99957059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43891348-G-A

99957078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43891367-C-T

99957100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43891389-C-G

99957117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43891406-T-C

99957137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43891426-G-A

99957182-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43891471-T-A

99957182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43891471-T-C

99957189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 43891481-G-A

99957229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43891520-G-A

99961602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43892688-A-G

99961613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43892699-T-A

99961614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43892700-C-T

99961919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43893077-C-T

99962177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43893463-A-G

99962203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43893489-G-C

http://identifiers.org/hco/10/GRCh38#99962215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43893501-A-C

99962278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43893536-T-A

99962278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43893536-T-C

99962279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43893537-G-A

99962279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43893537-G-T

99962288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43893546-C-T

99962793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43893736-T-C

99962908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43893835-C-T

99963479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43894164-G-A

99965049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43894694-C-T

99965256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43894850-T-C

99965268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43894862-T-G

99965286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43894887-A-G

99965331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43894931-C-T

99965386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43894991-A-G

99966543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43897694-C-G

99966543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43897694-C-T

http://identifiers.org/hco/10/GRCh38#99966594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#43897757-A-C

99966615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43897779-G-A

99967695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43898010-G-A

99967703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43898018-A-G

99967868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43898163-T-G

http://identifiers.org/hco/10/GRCh38#99969108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43899157-A-C

99969257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43899307-T-C

99969276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43899320-G-C

99969289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43899337-G-A

99969289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43899337-G-T

99969372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43899417-G-A

99969372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43899417-G-C

99969372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43899417-G-T

99971973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 43900671-T-A

http://identifiers.org/hco/10/GRCh38#99972038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43900732-A-C

99972148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43900842-T-A

99972148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43900842-T-C

http://identifiers.org/hco/10/GRCh38#99972150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43900844-A-C

99974314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43901553-G-A

99974314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43901553-G-C

99974386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43901668-T-A

99976595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43904681-T-C

99976650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43904733-T-C

99976696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43904772-C-T

99976756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43904832-A-T

http://identifiers.org/hco/10/GRCh38#99976775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43904851-A-C

99976775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43904851-A-G

http://identifiers.org/hco/10/GRCh38#99976783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43904864-C-A

99976783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43904864-C-T

http://identifiers.org/hco/10/GRCh38#99976795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43904876-A-C

99976872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43904944-C-T

99976901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43904966-C-T

99977200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43905246-G-T

http://identifiers.org/hco/10/GRCh38#99977242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43905276-A-C

99977254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43905288-A-G

99977480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43905529-C-T

99977800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43905754-C-T

99977941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43905892-T-A

99978026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43905985-T-C

99981504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43907244-A-G

99981707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43907443-G-A

99981809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43907605-T-C

99981809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43907605-T-G

99981815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43907620-T-G

99981911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43907708-A-G

99983480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43909168-T-C

99983548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43909235-G-A

99983548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43909235-G-C

http://identifiers.org/hco/10/GRCh38#99983690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43909334-A-C

99983721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43909370-T-C

http://identifiers.org/hco/10/GRCh38#99983732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43909379-C-A

99983732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43909379-C-T

99984096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43909691-G-A

99984100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 43909695-T-C

99984212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43909810-G-A

99984435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43910035-T-C

99984484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43910096-A-G

99984500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43910112-G-A

99985097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43910477-A-G

http://identifiers.org/hco/10/GRCh38#99985101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43910481-A-C

99987770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43911779-T-A

99987770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43911779-T-C

99987770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43911779-T-G

99987771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43911780-G-A

99987826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43911839-T-C

http://identifiers.org/hco/10/GRCh38#99987873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43911862-A-C

99993852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43914050-T-C

http://identifiers.org/hco/10/GRCh38#99994168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43914887-A-C

99994385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43915108-G-A

99994437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43915159-G-A

99994456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43915178-G-A

99994474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43915195-C-T

99994570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43915289-T-G

http://identifiers.org/hco/10/GRCh38#99994652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43915375-C-A

99994688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43915412-C-T

99994859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43915580-T-C

99996652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43916475-T-C

99996683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43916496-A-G

99996967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43916879-T-C

99997288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43917186-G-C

99997573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43917455-A-T

99997609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43917489-C-T

100000013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43918252-G-C

100000015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43918254-G-A

100000015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43918254-G-T

100000126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43918333-G-A

100000127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43918334-T-C

100000205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43918401-T-G

100000318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43918513-T-C

100000377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43918585-T-C

100000377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43918585-T-G

100000529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43918764-T-C

100000595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43918837-T-C

http://identifiers.org/hco/10/GRCh38#100000827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43918977-C-A

100001040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43919193-G-A

100001042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43919195-C-T

100001095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43919240-G-A

100001243-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43919386-A-T

100001260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43919403-A-G

100001273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43919416-G-A

100001827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43919495-A-G

http://identifiers.org/hco/10/GRCh38#100001851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43919529-A-C

http://identifiers.org/hco/10/GRCh38#100002130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43919804-A-C

100002130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43919804-A-G

100002540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43920143-C-G

http://identifiers.org/hco/10/GRCh38#100002628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43920219-A-C

100002628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43920219-A-T

100006241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43924844-T-C

http://identifiers.org/hco/10/GRCh38#100006257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43924860-A-C

100006564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43925129-T-A

100006641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43925206-T-C

100006678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43925242-C-G

100006678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43925242-C-T

100006731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 43925289-C-T

100007626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43925779-T-C

100007895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43926494-A-G

100008361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43927294-T-C

100009206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 43928051-G-A

http://identifiers.org/hco/10/GRCh38#100009593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43928345-C-A

100009635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron_variant, undefined
orthologous variants: 43928379-T-G

http://identifiers.org/hco/10/GRCh38#100009677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43928416-A-C

http://identifiers.org/hco/10/GRCh38#100009805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43928524-C-A

100009805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43928524-C-T

http://identifiers.org/hco/10/GRCh38#100009806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#43928525-C-A

100009806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30373
most severe consequence: intron variant
orthologous variants: 43928525-C-T