8808423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18364955-T-A

8808425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18364957-T-C

8808483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18365022-A-G

8808528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18365065-G-T

8808578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18365101-G-T

8808611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18365134-T-C

8808626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18365149-A-G

8808627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18365150-T-C

8808654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18365174-A-G

8808687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18365203-T-C

8808690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18365206-G-A

8808731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18365241-A-G

http://identifiers.org/hco/19/GRCh38#8809697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18366235-C-A

8809697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18366235-C-T

8809727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18366269-G-T

http://identifiers.org/hco/19/GRCh38#8809805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18366353-C-A

8809928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18366465-A-T

8810186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18366581-G-A

8810186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18366581-G-T

8810191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18366582-T-C

8810204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18366595-T-A

http://identifiers.org/hco/19/GRCh38#8810227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18366618-C-A

8810227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18366618-C-T

8810254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18366643-G-T

http://identifiers.org/hco/19/GRCh38#8810273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18366662-C-A

8810402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18366781-G-T

http://identifiers.org/hco/19/GRCh38#8810642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18366935-A-C

8810642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18366935-A-G

8810683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18366976-C-T

8810684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18366977-T-C

8810698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18366991-T-C

8810836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18367124-T-G

8810864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: 18367143-G-T

http://identifiers.org/hco/19/GRCh38#8810927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18367215-C-A

http://identifiers.org/hco/19/GRCh38#8811038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18367323-C-A

8811038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18367323-C-T

8811049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18367334-T-C

http://identifiers.org/hco/19/GRCh38#8811159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18367429-A-C

8811168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18367449-G-A

8811168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18367449-G-T

8811208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18367486-G-C

8811208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18367486-G-T

8811225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18367503-C-T

8811274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 18367556-C-G

8811401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18367683-C-T

8811440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18367722-G-A

8811440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 18367722-G-T

8811509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18367791-T-C

8811602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18367884-A-G

8811701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18367983-G-A

8811701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18367983-G-T

8811788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18368073-T-C

8811854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18368139-G-C

8811942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18368227-C-T

8812101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368382-A-G

8812102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368383-T-C

http://identifiers.org/hco/19/GRCh38#8812179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18368451-C-A

8812179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368451-C-G

8812195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368467-T-C

8812212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368484-G-A

8812212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368484-G-T

http://identifiers.org/hco/19/GRCh38#8812333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18368589-C-A

http://identifiers.org/hco/19/GRCh38#8812437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18368693-A-C

8812437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368693-A-G

http://identifiers.org/hco/19/GRCh38#8812449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18368705-C-A

8812449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368705-C-G

8812449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368705-C-T

8812452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368708-T-A

8812452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368708-T-C

http://identifiers.org/hco/19/GRCh38#8812464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18368720-C-A

8812464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368720-C-G

8812464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368720-C-T

http://identifiers.org/hco/19/GRCh38#8812508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18368760-C-A

http://identifiers.org/hco/19/GRCh38#8812519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18368771-C-A

8812519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368771-C-G

8812519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368771-C-T

http://identifiers.org/hco/19/GRCh38#8812536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18368784-C-A

8812536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368784-C-T

8812537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368785-A-G

8812573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18368821-T-C

8812581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18368829-G-C

8812588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18368836-T-C

8812634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18368882-G-A

8812634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18368882-G-T

8812639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18368887-C-T

8812646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 18368894-G-A

8812646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 18368894-G-C

8812646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 18368894-G-T

8812656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368904-G-A

8812656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368904-G-T

8812690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368944-G-T

8812708-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368962-T-A

8812708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368962-T-C

8812724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368978-G-C

8812724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368978-G-T

8812725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368979-G-A

8812729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18368983-C-G

http://identifiers.org/hco/19/GRCh38#8812750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18369004-C-A

8812750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18369004-C-T

8812752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18369006-A-G

8812759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18369014-G-A

8812904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18370781-T-G

8812945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18370818-G-A

8812985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18370856-C-G

8812985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18370856-C-T

8812990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18370861-T-C

8812993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18370864-T-A

http://identifiers.org/hco/19/GRCh38#8813009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18370880-C-A

8813009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18370880-C-T

8813019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18370890-G-A

8813019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18370890-G-T

http://identifiers.org/hco/19/GRCh38#8813039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18370907-A-C

8813039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18370907-A-G

8813040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18370908-T-C

8813162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 18370988-G-A

8813170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 18370996-C-T

8813259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18371087-G-A

8813259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18371087-G-T

8813271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18371102-A-T

http://identifiers.org/hco/19/GRCh38#8813291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18371115-C-A

8813765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18371264-C-T

8821093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18379146-A-G

8821134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18379174-T-C

8821317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18379352-G-T

8821358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18379389-G-A

8821375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18379406-A-G

8821389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18379420-A-T

8821409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18379443-A-T

8821426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18379461-G-A

8821426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18379461-G-C

8821426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18379461-G-T

8821610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18379557-G-A

http://identifiers.org/hco/19/GRCh38#8821660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18379600-C-A

8821685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 18379625-G-A

8821685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 18379625-G-T

http://identifiers.org/hco/19/GRCh38#8821694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18379634-A-C

8821694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379634-A-G

8821694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379634-A-T

8821722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379664-T-C

8821730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379672-T-G

http://identifiers.org/hco/19/GRCh38#8821743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18379685-C-A

http://identifiers.org/hco/19/GRCh38#8821753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18379695-C-A

8821759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379701-T-C

8821778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379719-G-A

8821778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379719-G-T

8821780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379721-G-A

8821780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379721-G-C

8821780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379721-G-T

8821796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379737-G-T

http://identifiers.org/hco/19/GRCh38#8821801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18379742-C-A

8821801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379742-C-T

http://identifiers.org/hco/19/GRCh38#8821812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18379753-C-A

http://identifiers.org/hco/19/GRCh38#8821862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18379803-C-A

8821862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379803-C-G

8821862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379803-C-T

8822047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379954-G-T

8822074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379981-G-A

8822074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18379981-G-C

8822091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 18379998-G-A

8822091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 18379998-G-C

8822098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 18380005-G-A

8822154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18380071-G-A

8822154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18380071-G-T

8822163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18380080-C-T

http://identifiers.org/hco/19/GRCh38#8822210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18380134-C-A

8822210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18380134-C-T

http://identifiers.org/hco/19/GRCh38#8822217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18380141-C-A

8822217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18380141-C-G

8822308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18380230-A-G

8822344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18380258-G-A

http://identifiers.org/hco/19/GRCh38#8822357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18380273-A-C

http://identifiers.org/hco/19/GRCh38#8822479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18380403-A-C

8822479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18380403-A-T

8822551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18380485-A-G

8822561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18380490-T-C

8822596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18380542-G-A

8822757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18380724-G-T

8822772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18380742-G-A

8822772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 18380742-G-C

http://identifiers.org/hco/19/GRCh38#8822822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18380794-A-C

8829559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18382976-T-C

8829845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383244-C-T

8830559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383741-A-G

8830569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383751-G-A

http://identifiers.org/hco/19/GRCh38#8830625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18383456-C-A

8830625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383456-C-T

8830630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383461-G-A

8830630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383461-G-C

8830667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383497-G-A

8830679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383514-G-A

8830679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383514-G-T

8830690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383540-A-G

8830694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383544-C-G

8830703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383553-C-T

8830709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383559-T-C

8830750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383600-C-T

8830924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383793-G-T

8831032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18383904-T-G

8831348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18384219-G-A

8831348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18384219-G-T

8831369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18384258-C-T

8831401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 18384290-T-A

8831401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 18384290-T-C

8831418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18384302-G-A

8831418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18384302-G-T

8831498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18384379-T-C

8831515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18384396-G-A

8831515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18384396-G-T

8831546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18384427-G-A

8831639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18384509-C-T

8831664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18384533-T-C

8831675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18384545-C-G

http://identifiers.org/hco/19/GRCh38#8831898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#18384678-C-A

8831898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18384678-C-T

8831979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18384744-G-T

8831994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18384753-C-G

8831994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18384753-C-T

http://identifiers.org/hco/19/GRCh38#8831995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#18384754-C-A

8831995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 18384754-C-T

8832052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 18384804-A-G

http://identifiers.org/hco/19/GRCh38#8832084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#18384826-C-A

8832084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 18384826-C-T

8832097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18384839-G-T

8832098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18384840-C-T

http://identifiers.org/hco/19/GRCh38#8832145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#18384850-C-A

8832169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18384857-G-A

8832169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18384857-G-T

http://identifiers.org/hco/19/GRCh38#8832191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18384879-C-A

8832191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 18384879-C-T

8832212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18384897-G-A

8832212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18384897-G-C

8832212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18384897-G-T

http://identifiers.org/hco/19/GRCh38#8832213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#18384898-C-A

8832213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18384898-C-T

8832231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 18384913-G-A

8832254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 18384935-A-G

8832285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 18384952-G-A

http://identifiers.org/hco/19/GRCh38#8832286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#18384954-C-A

8832286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 18384954-C-T

http://identifiers.org/hco/19/GRCh38#8832291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#18384959-C-A

8832291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 18384959-C-T

8832351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, undefined
orthologous variants: 18385005-C-T

8832397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 18385041-G-A

http://identifiers.org/hco/19/GRCh38#8832446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#18385068-A-C

8832453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 18385077-C-G

8832502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 18385130-T-C

http://identifiers.org/hco/19/GRCh38#8832566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#18385193-A-C

8832911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, undefined
orthologous variants: 18385204-T-A

8832911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, undefined
orthologous variants: 18385204-T-C

8832947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26422
most severe consequence: intron_variant, undefined
orthologous variants: 18385240-C-T