459947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 5 prime UTR variant
orthologous variants: 120271890-C-G

459947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 5 prime UTR variant
orthologous variants: 120271890-C-T

459986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 5 prime UTR variant
orthologous variants: 120271851-T-G

http://identifiers.org/hco/12/GRCh38#460090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120271753-C-A

460202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 5 prime UTR variant
orthologous variants: 120271655-C-T

460218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 5 prime UTR variant
orthologous variants: 120271638-G-T

460307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 5 prime UTR variant
orthologous variants: 120271569-G-T

460308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 5 prime UTR variant
orthologous variants: 120271568-G-A

460462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense variant
orthologous variants: 120271433-T-A

460462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense variant
orthologous variants: 120271433-T-C

460575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120271321-G-A

460575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120271321-G-T

http://identifiers.org/hco/12/GRCh38#460683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120271252-C-A

460683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120271252-C-G

460709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120271226-C-T

460820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120271151-C-G

461122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270896-C-T

461168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270871-G-C

461168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270871-G-T

461402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270666-A-G

http://identifiers.org/hco/12/GRCh38#461516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120270575-C-A

461540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270551-C-G

461561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270524-C-T

461710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120270407-G-A

http://identifiers.org/hco/12/GRCh38#461814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120270303-A-C

462379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120269830-C-T

http://identifiers.org/hco/12/GRCh38#462385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120269824-A-C

462385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120269824-A-T

462768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120268915-G-A

http://identifiers.org/hco/12/GRCh38#462922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120268730-A-C

http://identifiers.org/hco/12/GRCh38#463085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120268562-A-C

463825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120266745-C-G

463825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120266745-C-T

463842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120266728-A-G

463991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120266511-A-G

464023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120266483-C-T

464130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120266378-C-T

http://identifiers.org/hco/12/GRCh38#464230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120266299-A-C

464394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120266202-C-T

464500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120266069-G-T

465091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265543-G-A

465110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265529-G-T

465267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265413-A-G

466418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264299-C-T

467766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120262576-T-G

467786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120262555-G-A

http://identifiers.org/hco/12/GRCh38#467875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120262475-C-A

467875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120262475-C-T

468092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120262131-A-T

http://identifiers.org/hco/12/GRCh38#468516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120261749-C-A

468627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120261645-A-G

469473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120260303-G-C

469573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120260214-G-A

469713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120260072-G-A

470161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258746-G-A

470165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258719-A-G

470167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258717-A-G

470213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258667-C-T

470441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258479-C-T

470446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258473-G-A

470527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258397-T-C

470611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258349-G-A

470643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258321-C-T

470702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258261-A-G

473290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120257668-A-G

473474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120257076-G-T

473520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120257047-G-A

473797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120256846-G-C

474111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120256538-A-G

474347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120256341-C-T

475188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120256111-G-T

475460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120255861-G-A

475545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120255802-T-C

475545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120255802-T-G

475579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120255777-C-T

475711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120255673-T-C

475854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120255589-T-C

475867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120255576-C-T

479825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120253694-A-T

479836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120253683-A-G

http://identifiers.org/hco/12/GRCh38#480447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120253111-C-A

http://identifiers.org/hco/12/GRCh38#480520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120253085-A-C

480520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120253085-A-G

480589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120253015-G-T

480626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120252954-G-A

480740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120252846-G-A

480862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120252741-C-T

481278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120252307-A-G

http://identifiers.org/hco/12/GRCh38#481888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120251708-C-A

482055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120251588-G-A

482093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120251550-C-T

494779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120246523-G-T

494797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120246506-C-T

495003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120246344-G-A

http://identifiers.org/hco/12/GRCh38#495010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120246337-C-A

499843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120244613-G-A

499920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120244537-G-A

500127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120244469-G-T

500604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120243546-T-C

500604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120243546-T-G

500678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120243489-G-A

501163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120243079-T-C

501888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120242569-G-A

501944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120242524-C-T

502060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120242433-G-T

502228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120242284-G-A

502476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120242002-G-A

502476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120242002-G-T

503459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120241192-C-T

503759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120240885-A-T

http://identifiers.org/hco/12/GRCh38#503775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120240868-C-A

503775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120240868-C-G

503775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120240868-C-T

505139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

505139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

505347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

505637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120236798-T-C

505686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120236746-G-C

505903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120236543-G-A

505926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120236520-T-A

505978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120236468-G-A

505997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120236449-T-G

506050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120236401-A-G

http://identifiers.org/hco/12/GRCh38#506233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120236238-A-C

506239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120236137-A-G

506343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120236055-T-C

506345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120236053-G-A

506359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120236040-T-C

506406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120235995-T-G

507205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120235075-T-C

507456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120234714-C-T

507531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120234623-G-A

507851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120234362-C-T

http://identifiers.org/hco/12/GRCh38#507898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120234310-C-A

508046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120234130-A-G

508182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120234022-C-G

508234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120233972-C-G

508652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120233807-T-A

508653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120233806-T-G

508807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120233664-G-C

508925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120233587-G-A

509327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120233216-G-C

509327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120233216-G-T

509652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120232892-C-T

509943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120232617-C-T

510509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120231983-T-A

510509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120231983-T-G

510701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120231779-G-C

518947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120227712-A-G

http://identifiers.org/hco/12/GRCh38#519105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120227559-A-C

519502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120227177-C-G

519502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120227177-C-T

520269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120226723-C-G

520296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120226700-C-T

523221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120221183-C-G

523221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120221183-C-T

523259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120221155-G-A

523485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120220969-C-T

523488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120220968-A-G

523491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120220965-T-C

http://identifiers.org/hco/12/GRCh38#523788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120220759-C-A

523788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120220759-C-T

524324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120220433-T-C

524430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120220268-A-G

524476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120220198-G-A

524586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120220091-C-T

http://identifiers.org/hco/12/GRCh38#524920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120219853-A-C

524920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120219853-A-T

http://identifiers.org/hco/12/GRCh38#525827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120218797-C-A

525842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120218782-C-T

http://identifiers.org/hco/12/GRCh38#525852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120218772-C-A

525852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120218772-C-G

525890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120218736-T-G

526351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120218269-A-G

526352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120218268-A-T

526353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120218267-G-A

526487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120218153-C-T

526663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120218008-T-C

526728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120217950-A-G

526837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120217844-A-G

http://identifiers.org/hco/12/GRCh38#526898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120217786-C-A

527368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120217665-C-G

527491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120217548-G-C

527569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120217491-C-T

527909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120217191-G-T

527947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120217153-G-T

527952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120217148-G-C

528433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120215480-T-G

528535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120215349-C-T

528995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120214898-A-G

529063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120214834-C-T

529095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120214809-G-A

529132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120214760-C-T

529164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120214728-C-T

529291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120214611-T-G

529344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120214517-C-G

529519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120214357-C-T

530112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120214014-A-G

530853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120213104-C-T

531244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120212718-C-G

531244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120212718-C-T

http://identifiers.org/hco/12/GRCh38#531271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120212690-C-A

531284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120212677-A-T

531362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120212621-G-T

531789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120212497-G-A

531878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120212406-A-G

532410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120212162-G-A

532480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120212119-C-G

533523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120211533-G-A

533523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120211533-G-T

533589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120211470-C-T

533633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120211437-C-T

533854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120211226-T-A

533960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120210990-G-A

534028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120210936-C-G

534088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120210866-G-T

http://identifiers.org/hco/12/GRCh38#534186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120210713-C-A

534186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120210713-C-T

534344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120210568-G-T

534394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120210516-C-T

534490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120210419-G-A

534673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120210296-T-C

534921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120210134-C-T

http://identifiers.org/hco/12/GRCh38#535017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120210100-C-A

535017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120210100-C-T

http://identifiers.org/hco/12/GRCh38#535040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120210077-C-A

http://identifiers.org/hco/12/GRCh38#535041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120210076-C-A

535041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120210076-C-T

http://identifiers.org/hco/12/GRCh38#535043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120210074-A-C

http://identifiers.org/hco/12/GRCh38#535085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120210034-C-A

535085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120210034-C-G

535085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120210034-C-T

535246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120209870-C-G

http://identifiers.org/hco/12/GRCh38#535253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120209863-A-C

535253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120209863-A-G

http://identifiers.org/hco/12/GRCh38#535296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120209812-C-A

535296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209812-C-T

535395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209719-A-G

535395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209719-A-T

http://identifiers.org/hco/12/GRCh38#535406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120209708-C-A

535406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209708-C-G

535437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209682-A-G

http://identifiers.org/hco/12/GRCh38#535457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120209661-C-A

535490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209655-G-T

535535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209617-A-G

535567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120209585-C-T

536310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120208460-A-G

536907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120207639-T-C

537124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120207385-A-G

537625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120207142-T-G

538577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205859-A-G

538582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205854-G-A

538582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205854-G-T

538830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205675-T-C

539157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205519-T-G

539178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205498-C-G

539276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120205426-A-G

http://identifiers.org/hco/12/GRCh38#540354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120204503-C-A

540545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120204344-A-G

540620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120204281-G-A

540620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120204281-G-T

http://identifiers.org/hco/12/GRCh38#540621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120204280-C-A

541214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203986-C-G

541214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203986-C-T

541265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203939-G-A

541339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203873-C-T

541509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203550-T-C

541810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203265-G-C

541823-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203258-T-A

541823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203258-T-G

541898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203175-G-T

541899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120203169-C-T

542979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120202707-A-G

542979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120202707-A-T

http://identifiers.org/hco/12/GRCh38#543035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120202655-A-C

543035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120202655-A-T

543048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120202640-C-T

http://identifiers.org/hco/12/GRCh38#543062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120202626-C-A

543062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120202626-C-T

543103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120202601-C-G

543103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120202601-C-T

543128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120202576-A-G

543138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120202566-T-C

543138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120202566-T-G

http://identifiers.org/hco/12/GRCh38#543183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120202529-C-A

543183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120202529-C-T

http://identifiers.org/hco/12/GRCh38#543209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120202491-C-A

543209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120202491-C-G

544475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120201997-C-T

544533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120201934-T-G

http://identifiers.org/hco/12/GRCh38#544539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120201928-C-A

544539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120201928-C-T

544544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120201923-T-C

http://identifiers.org/hco/12/GRCh38#544553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120201914-C-A

544553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120201914-C-T

http://identifiers.org/hco/12/GRCh38#544786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120201695-C-A

544795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120201686-T-G

544876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120201600-G-A

544891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120201585-A-G

544984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120201493-C-T

http://identifiers.org/hco/12/GRCh38#544997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120201480-C-A

http://identifiers.org/hco/12/GRCh38#545067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120201426-A-C

545067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120201426-A-G

545069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120201424-C-G

http://identifiers.org/hco/12/GRCh38#545088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120201408-C-A

545088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120201408-C-T

545131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120201365-C-T

http://identifiers.org/hco/12/GRCh38#545141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120201355-C-A

545141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120201355-C-T

http://identifiers.org/hco/12/GRCh38#545155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120201341-C-A

545155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120201341-C-T

http://identifiers.org/hco/12/GRCh38#545219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120201286-C-A

545219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120201286-C-G

545252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120201251-G-A

545252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120201251-G-T

http://identifiers.org/hco/12/GRCh38#545281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120201218-A-C

545281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120201218-A-G

545318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120201184-T-C

545455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120201049-G-A

545508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120200997-T-C

546751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120200508-G-C

546780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120200470-G-C

http://identifiers.org/hco/12/GRCh38#546809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#120200447-C-A

546809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120200447-C-T

http://identifiers.org/hco/12/GRCh38#546812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#120200444-C-A

546815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120200441-T-C

546815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120200441-T-G

546870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120200399-G-A

546870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120200399-G-T

546898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120200122-G-A

546898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120200122-G-T

http://identifiers.org/hco/12/GRCh38#546902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120200118-C-A

546902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120200118-C-T

546923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120200097-C-T

546949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120200074-G-A

http://identifiers.org/hco/12/GRCh38#546955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#120200068-C-A

546955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120200068-C-T

547924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120199400-G-T

548002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120199335-T-C

548073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120199261-G-A

548076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120199258-G-A

548153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120199160-C-T

548304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120199016-A-G

548326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198996-A-G

548326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198996-A-T

548340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198980-G-A

548352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198968-C-G

548352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198968-C-T

548365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198962-G-A

http://identifiers.org/hco/12/GRCh38#548375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120198952-A-C

548375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198952-A-G

548375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198952-A-T

548405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198930-T-A

548408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198927-T-C

548428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198907-G-A

548428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198907-G-C

548428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120198907-G-T

549533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120196195-G-A

549679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120196062-C-G

549679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120196062-C-T

549708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120196028-G-A

549708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120196028-G-T

549728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120196012-A-G

549783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120195956-C-G

549801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120195938-C-T

549828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120195911-G-A

550000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195752-T-C

http://identifiers.org/hco/12/GRCh38#550003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120195749-C-A

550003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195749-C-G

550071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195587-G-A

550163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195434-G-T

550473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195031-A-G

550473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120195031-A-T

550621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194793-G-A

550621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194793-G-C

http://identifiers.org/hco/12/GRCh38#550780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120194699-C-A

550780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194699-C-T

http://identifiers.org/hco/12/GRCh38#550783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120194696-C-A

550783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194696-C-T

550785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194694-G-A

550785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194694-G-T

550874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194604-G-A

550874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194604-G-C

http://identifiers.org/hco/12/GRCh38#550894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120194552-C-A

550894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194552-C-T

550960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120194486-C-T

550990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120194456-G-A

551073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194378-G-A

551170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194272-T-C

551372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194128-G-A

551372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120194128-G-T

551652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193882-A-G

552239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193442-G-C

552307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193396-A-G

http://identifiers.org/hco/12/GRCh38#552333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120193371-A-C

552333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193371-A-G

552333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120193371-A-T

http://identifiers.org/hco/12/GRCh38#552405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120193332-C-A

http://identifiers.org/hco/12/GRCh38#552533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120193228-A-C

552590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120193164-A-G

552590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120193164-A-T

http://identifiers.org/hco/12/GRCh38#552614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120193140-C-A

552614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120193140-C-T

http://identifiers.org/hco/12/GRCh38#552711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120193072-C-A

552712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120193071-A-G

552712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120193071-A-T

552755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120193044-T-C

552792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120193031-T-A

552792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120193031-T-G

http://identifiers.org/hco/12/GRCh38#552794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120193029-C-A

552794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120193029-C-T

552833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120192993-T-A

552833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120192993-T-C

552833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120192993-T-G

552848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120192978-G-A

552848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120192978-G-T

552874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120192949-G-A

552874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120192949-G-T

http://identifiers.org/hco/12/GRCh38#552877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120192946-A-C

552877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120192946-A-G

552877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120192946-A-T

553048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120192581-G-A

553048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120192581-G-C

553048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120192581-G-T

http://identifiers.org/hco/12/GRCh38#553050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120192579-C-A

http://identifiers.org/hco/12/GRCh38#553058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120192571-A-C

553058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120192571-A-G

553142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120192514-T-C

553199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 120192454-G-T

553223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 120192430-C-T

http://identifiers.org/hco/12/GRCh38#553298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120192355-C-A

553299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120192354-C-G

553299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120192354-C-T

http://identifiers.org/hco/12/GRCh38#553378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120192284-C-A

553385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120192277-G-A

553450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120192212-G-A

553490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120192187-A-G

553754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120191929-G-C

554022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191668-A-G

554341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191482-C-T

554405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120191366-A-G

556464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120187427-T-C

556498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120187399-T-C

http://identifiers.org/hco/12/GRCh38#556528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120187386-C-A

556656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120187261-C-G

556656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120187261-C-T

556703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120187214-A-G

556704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120187213-G-C

556777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120187140-T-C

556777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120187140-T-G

556899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120187037-G-A

556899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120187037-G-C

556899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120187037-G-T

http://identifiers.org/hco/12/GRCh38#556963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120186984-C-A

556963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186984-C-T

557106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186873-T-G

557423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186513-G-A

557574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186377-G-A

557574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186377-G-T

557622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120186331-C-T

557676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120186277-G-A

557744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120186209-G-A

557744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120186209-G-C

557744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120186209-G-T

557765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186188-A-G

http://identifiers.org/hco/12/GRCh38#557779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120186174-C-A

557779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186174-C-T

557786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186168-G-A

557786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186168-G-T

557811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186148-A-G

557835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186126-G-A

557835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120186126-G-T

http://identifiers.org/hco/12/GRCh38#557928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120186055-C-A

http://identifiers.org/hco/12/GRCh38#557996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120185961-C-A

557996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120185961-C-G

557996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120185961-C-T

557999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120185954-C-T

558026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120185927-G-A

558029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120185924-A-G

558093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120185859-A-G

558514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120184229-C-T

558662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 120184081-G-T

558687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120184056-G-C

558688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120184055-A-G

558709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120184039-G-C

558709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120184039-G-T

558710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120184038-G-A

558710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120184038-G-T

http://identifiers.org/hco/12/GRCh38#558737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120184011-C-A

558737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120184011-C-T

558754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183996-G-A

558754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183996-G-T

http://identifiers.org/hco/12/GRCh38#558780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120183979-C-A

558780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183979-C-T

http://identifiers.org/hco/12/GRCh38#558785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120183974-C-A

558785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183974-C-T

558826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183949-C-G

558826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183949-C-T

558882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183903-C-T

559160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183660-T-C

http://identifiers.org/hco/12/GRCh38#559179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120183643-C-A

559179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183643-C-G

559179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183643-C-T

559190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183633-G-A

559255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183602-C-T

559289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120183570-C-G

559289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120183570-C-T

559327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120183532-G-A

559479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183374-G-A

559772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183081-T-C

559795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183055-C-T

559799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120183051-G-A

559858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120182994-G-T

560322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120182050-C-T

560406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181969-C-T

560410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181965-A-G

560435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181940-G-A

560739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181639-G-A

http://identifiers.org/hco/12/GRCh38#560772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120181604-C-A

560772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181604-C-G

560772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181604-C-T

561222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120181046-T-C

http://identifiers.org/hco/12/GRCh38#561453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120180768-C-A

561453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180768-C-T

561465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180756-G-A

561465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180756-G-T

561468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180753-G-A

561468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180753-G-T

561559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180682-A-G

http://identifiers.org/hco/12/GRCh38#561572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120180669-C-A

http://identifiers.org/hco/12/GRCh38#561583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120180658-C-A

561583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180658-C-T

http://identifiers.org/hco/12/GRCh38#561587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120180654-A-C

http://identifiers.org/hco/12/GRCh38#561588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120180653-C-A

561588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180653-C-T

561611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180624-G-A

561611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180624-G-C

562216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180084-T-C

562226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180072-C-T

562237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180061-G-T

http://identifiers.org/hco/12/GRCh38#562275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120180026-C-A

562275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180026-C-T

562284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180017-T-C

562284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180017-T-G

562287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180013-G-A

562287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120180013-G-T

562377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179922-G-A

562377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179922-G-T

http://identifiers.org/hco/12/GRCh38#562380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120179919-C-A

562380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179919-C-T

http://identifiers.org/hco/12/GRCh38#562495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120179813-A-C

562495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179813-A-G

562505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179803-G-A

562505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179803-G-C

562505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179803-G-T

562525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179787-G-A

562525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179787-G-T

562560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179770-G-C

562560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179770-G-T

562646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179720-A-G

562646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179720-A-T

562794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179614-C-T

http://identifiers.org/hco/12/GRCh38#562810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120179598-C-A

562810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179598-C-G

562835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179572-G-T

562857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179520-C-T

http://identifiers.org/hco/12/GRCh38#562899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120179487-C-A

562899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179487-C-T

562999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179391-A-G

563053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179357-T-C

563064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179346-A-G

http://identifiers.org/hco/12/GRCh38#563133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120179306-C-A

563159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179280-C-T

563168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179271-G-A

563168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179271-G-T

563246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179195-G-A

563246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179195-G-T

563299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179143-A-G

563319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179123-G-A

563319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179123-G-T

http://identifiers.org/hco/12/GRCh38#563344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#120179097-C-A

563344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179097-C-T

563345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179096-G-A

563345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24137
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120179096-G-T