128267187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: 5 prime UTR variant
orthologous variants: 127318896-G-A

128267187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: 5 prime UTR variant
orthologous variants: 127318896-G-C

128267212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: 5 prime UTR variant
orthologous variants: 127318907-A-T

128267313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: 5 prime UTR variant
orthologous variants: 127318936-T-C

128267313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: 5 prime UTR variant
orthologous variants: 127318936-T-G

128267477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127319074-G-A

128267477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127319074-G-T

128267542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127319120-G-T

128267581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127319152-G-A

128267581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127319152-G-T

128267622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127319194-T-A

128267622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127319194-T-C

128267622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127319194-T-G

128267812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127319363-G-A

128267960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127319402-A-G

128268342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127319681-C-G

128268342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127319681-C-T

128268600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127319850-A-G

128268831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127320098-T-C

128269859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127321061-G-C

128270063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127321261-C-T

128273770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127324200-T-C

128273968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127324408-T-C

128274052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127324478-T-C

128274189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127324600-T-C

128274444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127324799-C-T

128276636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127327189-A-G

128276700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127327260-G-C

128276962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127327474-A-G

128276962-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127327474-A-T

http://identifiers.org/hco/12/GRCh38#128277420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127327947-A-C

128277420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127327947-A-G

128277466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127327990-G-A

128277954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127328989-A-G

128278301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127329299-C-T

128278883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127329781-C-T

128278971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127329853-G-A

128279057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127329913-T-C

128279063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127329919-T-A

128279063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127329919-T-C

128286866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127332323-G-A

128286866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127332323-G-T

128287866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127333120-G-A

128287866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127333120-G-T

128287867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127333121-A-G

128288035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127333268-C-T

128288048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127333281-T-C

128289539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127334066-C-T

128289613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127334120-C-T

128289711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127334213-A-G

128289723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127334232-T-C

128289982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127334505-T-C

128289993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127334516-T-G

128291141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127335923-A-G

128291146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127335928-C-T

http://identifiers.org/hco/12/GRCh38#128291297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127336048-C-A

128291336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127336086-G-A

128291627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127336343-G-A

128291648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127336355-A-G

128291739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127336406-G-A

128292105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127336764-G-A

128292266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127336925-T-C

128292362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127337025-G-A

128293189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127338429-G-A

128293641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127338864-A-G

128293652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127338874-T-C

128293781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127339011-A-G

128293907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127339136-G-C

128294040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127339277-G-T

128297030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127340214-T-C

128297230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127340396-G-T

http://identifiers.org/hco/12/GRCh38#128297248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127340414-C-A

128297614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127340758-T-C

128298751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127342455-T-C

128298784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127342487-G-A

128298875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127342587-T-G

128298974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127342688-G-A

128299953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127343509-G-A

128299953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127343509-G-T

128302936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127344439-C-T

128302981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127344484-G-A

128303010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127344497-C-G

128303230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127344707-G-A

http://identifiers.org/hco/12/GRCh38#128303280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127344758-C-A

128305261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127344861-A-G

128305515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127345111-C-T

http://identifiers.org/hco/12/GRCh38#128305703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127345307-A-C

128305794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127345402-A-G

128306602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127346033-A-G

128306607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127346038-T-A

128306607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127346038-T-G

128306631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127346062-C-T

128306767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127346205-G-T

128306932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127346379-G-C

128307116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127346667-C-T

128307156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127346737-C-T

128307272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127346831-G-T

128307278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127346837-T-C

128307293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127346852-G-A

128307300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127346859-G-A

128307321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127346880-A-G

128307424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127346983-T-C

128307929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127347475-C-T

128308020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127347584-G-A

128308045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127347610-G-A

128308169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127347913-C-T

http://identifiers.org/hco/12/GRCh38#128308656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127348331-C-A

128308656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127348331-C-T

128308764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127348406-C-G

128308764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127348406-C-T

128308765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127348407-G-A

128308765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127348407-G-T

128308894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127348523-G-C

128308894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127348523-G-T

128311250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356447-C-T

128311331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356501-A-G

128311403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356584-T-C

128311412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356593-C-T

128311518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356690-G-A

128311585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356767-A-G

128311593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356775-G-A

128311593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356775-G-T

128311629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356811-T-C

128311637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356819-C-G

128311651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356833-A-G

128311652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356834-G-A

128311668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356847-G-A

128311675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356854-C-G

128311675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356854-C-T

128311728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356891-C-T

128311797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127356960-T-A

128311851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127357003-A-G

128312041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127357181-C-T

128313767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127359481-G-A

128313796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127359511-G-A

128313934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127359664-A-G

http://identifiers.org/hco/12/GRCh38#128314087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127359840-C-A

128314242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127359997-A-T

128314280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127360039-A-G

128314480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127360251-A-T

http://identifiers.org/hco/12/GRCh38#128314499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127360310-C-A

128314499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127360310-C-T

128316727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127362441-T-G

128316771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127362485-T-C

128317091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127362814-G-A

http://identifiers.org/hco/12/GRCh38#128317236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127362947-C-A

128317377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127363085-G-A

128317387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127363095-A-G

128319928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127365382-G-A

128319939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127365393-G-C

128319972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127365424-T-C

128320015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127365480-T-C

128320122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127365568-T-C

128322073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127366640-G-A

128322147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127366715-T-C

128322274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127366832-C-T

128322309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127366867-C-T

128322473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127367006-G-A

128322474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127367007-G-A

128322476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127367009-C-G

http://identifiers.org/hco/12/GRCh38#128322604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127367120-C-A

128322604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127367120-C-T

128322948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127367372-A-G

http://identifiers.org/hco/12/GRCh38#128323576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127367982-C-A

128323576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127367982-C-T

128323678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127368085-A-G

128323743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127368151-G-A

128323932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127368314-T-C

128325525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127372072-C-T

128325783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127372299-T-G

128325967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127372445-G-A

128326036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127372506-A-G

128326211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127372643-C-T

128326320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127372735-A-G

128326539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127372952-C-T

128326635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127373010-G-A

128326695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127373075-G-T

128326811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127373177-C-G

128326811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127373177-C-T

128327015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127373411-C-T

http://identifiers.org/hco/12/GRCh38#128327020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127373419-C-A

128327020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127373419-C-T

128329331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127375924-T-C

128329686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127376270-G-C

128332616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127377892-C-T

128332845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127378063-G-C

128333597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127378844-G-C

128334395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127379311-T-A

128335309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127380637-C-T

128335962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127382145-T-C

128336182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127382360-G-A

http://identifiers.org/hco/12/GRCh38#128336199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127382377-C-A

128336199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127382377-C-T

http://identifiers.org/hco/12/GRCh38#128336316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127382494-A-C

128336316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127382494-A-G

128336557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127382743-T-C

128336558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127382744-G-C

128336845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127383090-T-C

128336972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127383173-T-G

128336998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127383199-T-C

128337446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127383761-A-G

128337621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127383892-A-G

128337941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127384202-T-C

128337949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127384210-C-T

128337955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127384216-C-G

http://identifiers.org/hco/12/GRCh38#128338130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127384394-C-A

128338193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127384457-G-A

128338725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127387388-C-T

128338869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127387551-C-T

128338900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127387574-G-A

128339050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127387748-G-A

128339070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127387766-T-G

128339165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127387852-A-G

128339173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127387860-C-T

128339250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127387932-G-A

128339321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127387999-G-T

128339374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127388056-A-G

128340207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127388482-G-T

128340226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127388500-A-G

128340279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127388551-C-T

128340296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127388568-C-T

128341339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127389394-C-T

128347909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127392689-T-C

128348497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127393254-G-C

128349024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127393629-G-A

http://identifiers.org/hco/12/GRCh38#128349035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127393635-A-C

128359757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127395324-T-C

128359993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127395550-A-G

128359997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127395554-T-C

128360035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127395596-T-C

128361032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127395915-A-G

128361090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127395977-C-T

128361600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127396442-G-T

128361700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127396569-G-A

128361700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127396569-G-C

128362149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127397253-A-G

128362229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127397313-G-A

128362252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127397337-G-C

128362289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127397374-G-A

128362289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127397374-G-C

128365648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127401011-T-C

128365988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127401341-G-T

128366007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127401360-C-T

128366100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127401457-C-T

128366133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127401491-C-G

128366133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127401491-C-T

128366145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127401503-C-T

128366363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127401696-T-A

http://identifiers.org/hco/12/GRCh38#128366950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127403047-C-A

128367149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127403219-G-A

128367338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127403386-G-T

128367516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127403492-T-C

128372025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127404778-C-T

128372255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127404972-A-G

128372570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127405309-G-A

128372570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127405309-G-T

128372798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127406638-A-G

128372960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127406783-G-T

128373206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127407003-G-A

128373425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127407212-A-T

128373539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127407322-A-G

128373567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127407352-C-G

128373582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127407367-C-T

128375893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127408963-G-A

128376011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127409083-G-A

128381101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127412624-C-T

128381152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127412675-A-G

128381209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127412739-C-T

128381322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127412858-T-G

128381821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127413354-C-T

128381885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127413431-G-A

128381937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127413479-G-A

128382032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127413558-G-T

128382958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127415530-A-G

128382970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127415542-A-G

128382974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127415546-G-A

128383000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127415572-G-A

128383000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127415572-G-T

128383340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127415936-C-T

128383488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127416064-C-G

128383911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127416476-G-A

128383911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127416476-G-C

128387950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127418394-G-A

128387961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127418404-G-A

128388060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127418485-G-C

http://identifiers.org/hco/12/GRCh38#128388198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127418630-C-A

128394725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: -C-T

128396171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127421886-T-C

128397991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127422840-T-C

128398966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127424134-C-T

128399048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127424213-G-A

128399780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127424940-T-C

128399781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127424941-T-A

128399781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127424941-T-C

128402702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127426383-C-T

128402714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127426395-G-A

128402714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127426395-G-C

128402810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127426457-C-T

128402814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127426467-G-A

128402823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127426476-T-C

http://identifiers.org/hco/12/GRCh38#128402985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#127426636-C-A

128403085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127426738-A-G

128403085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127426738-A-T

128403389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127427037-G-A

128403976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127427895-G-A

128403983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127427900-C-G

128404375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127429195-T-C

128404381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127429201-T-C

128404832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127429461-A-G

http://identifiers.org/hco/12/GRCh38#128404857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127429486-C-A

128405189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127429805-A-G

128405189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127429805-A-T

128405191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127429807-G-T

128408780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127433099-G-A

128408908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127433222-G-C

128408910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127433224-G-A

128408989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127433306-G-T

128409176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127433479-T-C

128409259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127433547-G-A

128409324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127433611-C-T

128409515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127433791-T-C

128409874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127434589-C-T

128409907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127434622-G-C

128409966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127434675-A-G

http://identifiers.org/hco/12/GRCh38#128409968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127434677-C-A

128409968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127434677-C-T

128409980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127434689-C-G

128409980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127434689-C-T

128410104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127434850-A-G

http://identifiers.org/hco/12/GRCh38#128410210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127434962-C-A

128410313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127435023-G-A

128410313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127435023-G-C

128410337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127435052-C-T

128410590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127435237-G-A

http://identifiers.org/hco/12/GRCh38#128410618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127435265-A-C

128410665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127435333-A-G

128410684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127435352-G-A

128410688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127435356-G-A

128414281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127436113-A-T

128414735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: 127436622-T-A

128414737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: 127436624-G-A

128415157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: 127437041-A-T

128415158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: 127437042-G-A

128415158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: 127437042-G-T

128415201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437085-C-T

128415204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437088-G-A

128415204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437088-G-C

128415204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437088-G-T

128415207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437091-G-A

128415207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437091-G-T

http://identifiers.org/hco/12/GRCh38#128415238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127437122-C-A

128415238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437122-C-T

http://identifiers.org/hco/12/GRCh38#128415317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127437201-C-A

128415317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: 127437201-C-T

128415321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437205-T-A

128415321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437205-T-C

http://identifiers.org/hco/12/GRCh38#128415353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127437237-A-C

128415353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: 127437237-A-G

http://identifiers.org/hco/12/GRCh38#128415354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127437238-C-A

128415354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437238-C-T

128415363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437247-G-T

128415475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: 127437359-G-T

http://identifiers.org/hco/12/GRCh38#128415498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127437382-C-A

128415498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: 127437382-C-G

128415498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437382-C-T

128415570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437454-G-A

128415570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437454-G-C

128415570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127437454-G-T

128415627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 127437511-G-A

http://identifiers.org/hco/12/GRCh38#128415634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127437518-C-A

128415664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127437548-T-A

128415677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127437561-T-A

128415677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127437561-T-C

128416473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127438684-C-T

http://identifiers.org/hco/12/GRCh38#128416642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127438883-A-C

128416642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127438883-A-G

128416664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127438905-T-A

128416830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127439168-A-G

128416867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127439201-C-T

128417010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127439264-G-A

128417059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127439310-G-A

128417069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127439320-A-G

128417336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127439573-C-G

128417336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127439573-C-T

128417342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127439579-C-T

http://identifiers.org/hco/12/GRCh38#128417369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127439610-C-A

128417776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127439922-A-G

128417813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127439959-T-C

http://identifiers.org/hco/12/GRCh38#128418268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127440374-A-C

128425705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127446735-A-G

128425705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127446735-A-T

128426100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127447050-G-A

128426100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127447050-G-T

128426108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127447058-T-C

128426177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127447102-G-A

128426451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127447402-G-A

128426451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127447402-G-T

128426596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127447554-A-G

128427376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127449259-A-G

128427626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127449456-G-A

128427626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127449456-G-T

128427680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127449488-C-T

128427699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127449506-G-A

128428025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127449817-C-T

128428060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127449852-C-T

128428199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127449973-G-C

http://identifiers.org/hco/12/GRCh38#128428704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127450397-C-A

128428730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127450428-T-C

128428730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127450428-T-G

128428832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127450529-T-A

128428931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127450632-T-C

128429185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127450867-G-A

128429202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127450884-A-G

128429232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127450903-A-G

128429634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127451231-C-G

http://identifiers.org/hco/12/GRCh38#128430064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127451629-C-A

128430064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127451629-C-T

http://identifiers.org/hco/12/GRCh38#128433546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127452258-C-A

128433546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127452258-C-G

http://identifiers.org/hco/12/GRCh38#128433696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127452386-C-A

128433814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127452487-G-A

128441426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127452885-C-T

128441678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127453140-T-A

128441704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127453166-A-G

128445644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127455656-T-G

128445928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127455947-T-C

128446073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127456100-A-G

128446208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127456222-A-G

128446271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127456283-G-A

128446372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127456378-C-T

128446486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127456469-A-G

128447007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127456948-G-T

128447175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127457084-T-C

128448131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127458630-A-G

128448163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127458844-T-C

128448340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127459042-G-A

128448383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127459083-A-G

128448479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127459167-G-A

128448494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127459183-G-A

128448610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127459245-C-G

128448781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127459394-G-A

128448812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127459420-T-C

128448872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127459477-C-T

128449343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127459642-C-T

128449378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127459676-G-T

128449759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127460028-C-T

128450778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127460405-C-T

128450970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127460600-G-A

128451002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127460621-T-C

http://identifiers.org/hco/12/GRCh38#128451021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127460640-C-A

http://identifiers.org/hco/12/GRCh38#128451053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127460672-A-C

128451163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127460760-G-A

128451339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127460987-C-T

128451462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127461101-G-A

128451487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127461126-G-A

128451487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127461126-G-T

128451491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127461130-G-A

128451651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127461282-G-A

128451651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127461282-G-T

http://identifiers.org/hco/12/GRCh38#128451721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127461344-C-A

128451721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127461344-C-T

128451826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127461447-C-G

128451826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127461447-C-T

128451852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127461473-A-G

128453936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127465493-C-T

128454158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127466219-T-C

128454393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127466422-A-G

128454517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127466542-T-G

128454602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127466621-C-T

128454642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127466661-C-T

128454676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127466694-A-G

128454966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127468955-T-C

128455193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127469187-G-A

http://identifiers.org/hco/12/GRCh38#128455337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127469331-A-C

128455356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127469353-G-A

128455411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127469405-G-C

128455470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127469464-A-G

http://identifiers.org/hco/12/GRCh38#128455494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127469488-C-A

128455505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127469499-G-A

128455676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127469615-A-G

http://identifiers.org/hco/12/GRCh38#128455738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127469674-C-A

128455828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127469765-G-A

128455828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127469765-G-C

128455864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127469798-C-T

128455932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127469863-G-A

128456240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127470181-G-A

128456291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127470219-A-G

128456291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127470219-A-T

128460521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127475028-T-C

128460567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127475069-G-A

128460578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127475080-T-C

128460907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127475304-C-T

128461217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127475636-A-G

128467011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127479523-A-G

128467288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127480878-T-C

128467296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127480886-G-T

128467403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127480989-G-T

http://identifiers.org/hco/12/GRCh38#128467414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127481000-C-A

128467489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127481076-T-C

128467507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127481121-C-G

128467514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127481130-G-T

128467576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127481186-G-A

128470469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127483011-T-G

http://identifiers.org/hco/12/GRCh38#128470739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127483594-C-A

128470739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127483594-C-T

128470855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127483706-G-A

128470855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127483706-G-C

128471007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127483863-G-T

128471066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127483901-T-C

128471135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127483970-G-A

128471497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127484491-G-A

128474308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127487919-A-G

128474486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488092-A-G

128474641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488245-C-G

128474641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488245-C-T

128474646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488250-A-G

128474648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488252-T-A

128474676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488279-G-A

128474748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488358-T-A

128474805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488401-G-A

128474894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488476-G-C

128474918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488499-C-T

128474989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488565-G-A

128475022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488602-G-A

128475093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488658-T-G

http://identifiers.org/hco/12/GRCh38#128475158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127488796-C-A

128475178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488816-C-T

128475188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488826-G-A

http://identifiers.org/hco/12/GRCh38#128475203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127488832-C-A

128475272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127488897-G-A

128476316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127491409-C-T

128476528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127491604-T-G

128476933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127491931-A-G

128478019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127492548-A-G

128478048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127492577-A-T

128478528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127493058-C-T

128478878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127493357-A-G

128478946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127493428-A-G

128479610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127493722-A-G

128479690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127493795-G-A

128480167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127494306-C-T

128480368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127494525-C-G

http://identifiers.org/hco/12/GRCh38#128480445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127494610-A-C

128480837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127495232-G-A

128486651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127498994-C-T

128490818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127503927-G-A

128490864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127503973-A-G

128491182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127504262-G-A

128491216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127504296-T-A

128491332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127504401-G-A

128491347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127504429-A-T

128491547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127504607-G-T

http://identifiers.org/hco/12/GRCh38#128491552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127504612-C-A

128491592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127504640-C-T

http://identifiers.org/hco/12/GRCh38#128501614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127506907-C-A

128501619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127506911-G-A

128501914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127507265-T-C

128501930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127507281-G-A

128501934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127507285-G-A

128502045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127507488-A-T

128502322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127507730-C-T

128502400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127507798-G-A

128502534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127508369-G-A

128502790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127508558-A-G

http://identifiers.org/hco/12/GRCh38#128503060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127508831-A-C

128503060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127508831-A-G

128503433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127509195-C-T

128503625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127509324-G-A

128507293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127510855-G-C

128507362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127510921-A-G

128507406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127510957-T-C

128507408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127510959-T-C

128507439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127511002-C-T

128507444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127511007-C-T

http://identifiers.org/hco/12/GRCh38#128507713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127511267-C-A

128507745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127511298-C-G

128507745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127511298-C-T

128507850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127511394-T-C

128510464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127513786-A-G

128510474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127513796-G-A

128510476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127513799-G-A

128510658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127513964-G-A

128510912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127514218-G-C

128511120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127514397-A-G

128511260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127514542-T-C

128511370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127514636-C-T

128511512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127514765-G-A

128513413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127517958-G-T

http://identifiers.org/hco/12/GRCh38#128513495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127518035-C-A

128513495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127518035-C-T

128513762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127518280-C-T

http://identifiers.org/hco/12/GRCh38#128513806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127518332-C-A

128513894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127518434-C-G

128513943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127518475-A-T

128514234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127518740-G-T

128517789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127519025-G-A

128518044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127519273-C-T

128518276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127519498-G-A

128518375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127519598-G-A

128518375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127519598-G-T

128518627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127520092-A-G

128518663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127520120-C-G

128518663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127520120-C-T

128518779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127520351-A-G

128518780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127520352-C-T

128519098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127520651-A-G

128519098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127520651-A-T

128519114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127520667-A-G

128524204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127524893-C-T

128524424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127525102-C-G

128524444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127525122-T-G

128524813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127525478-A-G

128524987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127525597-G-A

http://identifiers.org/hco/12/GRCh38#128525218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127525814-C-A

128526531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127527041-G-T

128527264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127527720-G-A

128527264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127527720-G-T

128527312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127527774-C-G

128527570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127528019-C-T

http://identifiers.org/hco/12/GRCh38#128528569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127528715-A-C

128528569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127528715-A-G

128531076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127531294-A-G

128531581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127531785-G-A

128531581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127531785-G-T

http://identifiers.org/hco/12/GRCh38#128531844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127532085-C-A

128534083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127534924-G-A

128534251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127535065-C-T

128534263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127535077-A-G

http://identifiers.org/hco/12/GRCh38#128534264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127535078-C-A

128534264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127535078-C-T

128534265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127535079-G-A

128534265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127535079-G-C

128534270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127535084-T-G

128534468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127535295-T-A

128534477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127535305-C-T

128534505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127535331-G-T

128534727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127537210-C-G

128534812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127537295-C-T

http://identifiers.org/hco/12/GRCh38#128534840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127537323-C-A

128534873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127537355-G-A

128534873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127537355-G-C

128534877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127537359-A-G

http://identifiers.org/hco/12/GRCh38#128544098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127540109-C-A

http://identifiers.org/hco/12/GRCh38#128544146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127540150-C-A

128544146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127540150-C-T

http://identifiers.org/hco/12/GRCh38#128544150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127540154-C-A

128544150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127540154-C-T

http://identifiers.org/hco/12/GRCh38#128544205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127540198-A-C

128544205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127540198-A-G

128544429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127540366-G-A

128544458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127540394-G-A

http://identifiers.org/hco/12/GRCh38#128544475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127540410-A-C

128544583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127540505-G-T

128544671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127540578-C-G

128544885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127540790-A-G

128545983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127542689-C-T

128546046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127542744-T-C

128546117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127542812-C-T

128546124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127542819-A-G

128546129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127542831-T-C

128546154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127542856-C-T

128546214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127542901-T-C

128546262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127542947-C-T

128547003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127545219-G-A

128547252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127545462-A-G

128547335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127545532-G-A

128547634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127545607-T-A

128550787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127546542-A-G

http://identifiers.org/hco/12/GRCh38#128550876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127546633-C-A

http://identifiers.org/hco/12/GRCh38#128551031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127546776-C-A

128551124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127546855-A-T

http://identifiers.org/hco/12/GRCh38#128551181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127546916-C-A

128551385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127547110-T-C

128551507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127547267-C-T

128551521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron_variant, undefined
orthologous variants: 127547281-G-T

128551830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127547575-C-T

128552073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127547818-C-T

128552078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127547823-T-G

128552177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127547906-C-T

128552411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127548131-C-T

128552542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127548261-G-A

128554615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127549735-T-C

128554647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127549766-G-C

128554669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127549789-C-T

128554732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127549870-C-T

128554787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127549926-G-T

128554986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127550112-T-A

128554986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127550112-T-C

128555001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127550127-C-T

128555028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127550154-G-A

128555451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127550546-A-G

http://identifiers.org/hco/12/GRCh38#128555508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127550594-A-C

128556788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127552235-C-T

128556885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127552354-G-A

128557076-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127552550-T-A

128557152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127552606-G-A

128557152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127552606-G-C

128557256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127552663-G-C

128557277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127552682-C-T

http://identifiers.org/hco/12/GRCh38#128557348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127552755-C-A

128557435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127552838-A-G

128561208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127553644-T-A

128561208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127553644-T-C

128561299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127553734-T-C

128561649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127554066-T-C

128561711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127554120-G-A

128561782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127554186-C-T

128561894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127554317-T-C

128561996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127554464-G-C

128562086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127554548-T-C

http://identifiers.org/hco/12/GRCh38#128562195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127554670-C-A

128562266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127554748-G-A

128562702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127555163-C-T

http://identifiers.org/hco/12/GRCh38#128562756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127555213-A-C

http://identifiers.org/hco/12/GRCh38#128562964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127555421-C-A

http://identifiers.org/hco/12/GRCh38#128562972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127555429-A-C

128563075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127555515-A-G

128563086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127555527-G-A

128563108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127555548-G-A

128563126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127555566-T-C

128563129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127555569-C-T

128563366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127555785-T-C

128563373-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127555792-T-G

128565230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127558332-C-T

128565506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127558530-T-C

128565527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127558551-T-C

128565582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127558571-A-G

128565626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127558585-T-G

128566501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127559420-T-C

128566656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127559566-T-C

128566739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127559610-T-C

128569090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127561154-G-A

128569182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127561244-G-A

128569211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127561264-T-C

128569328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127561377-A-G

128569420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127561467-G-A

128570146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127562223-A-G

128570274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127562350-A-G

128570351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127562427-G-A

128570351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127562427-G-C

128570611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127562657-G-A

128570651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127562702-C-T

128571128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127563184-G-A

128571149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127563200-G-A

128571246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127563290-T-C

128571495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127563543-A-G

128571495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127563543-A-T

128571568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127563616-C-T

128571759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127563778-T-C

128577747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127565615-T-C

128578142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127565963-C-T

http://identifiers.org/hco/12/GRCh38#128578269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127566089-A-C

128578471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127566368-C-T

128578485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127566382-A-G

128578539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127566430-G-T

128578558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127566449-A-G

128579146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127567159-G-A

128579267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127567261-G-A

128579267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127567261-G-T

128579354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127567355-G-A

128581465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127568200-G-A

128581689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127568429-C-T

128581730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127568468-C-T

128581798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127568523-C-G

128581798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127568523-C-T

128581874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127568596-T-C

128586616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127570260-A-G

http://identifiers.org/hco/12/GRCh38#128587323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127571884-C-A

128587476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127572007-T-G

128593522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127573205-G-A

128593576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127573257-C-T

128593627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127573309-C-T

128593628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127573310-G-A

http://identifiers.org/hco/12/GRCh38#128593704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127573380-C-A

128593704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127573380-C-T

128593862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127573606-C-G

128593905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127573648-A-G

128594017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127573766-A-G

128594084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127573833-G-A

128594244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127573971-G-C

http://identifiers.org/hco/12/GRCh38#128594513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127574135-A-C

128594803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127574417-G-A

128594837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127574451-A-G

http://identifiers.org/hco/12/GRCh38#128594888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127574502-C-A

128595148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127574708-T-C

128595380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127574925-G-A

128595423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127574968-G-A

128600628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127576274-A-G

128601118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127576758-G-A

128601163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127576811-C-T

http://identifiers.org/hco/12/GRCh38#128601165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127576813-C-A

128601429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127577055-G-A

128601448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127577079-A-G

128601448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127577079-A-T

128601580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127577188-G-A

128601580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127577188-G-C

128601629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127577258-A-G

128601629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127577258-A-T

128601647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127577276-A-G

128609989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127580042-C-T

128610015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127580061-C-G

128610016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127580062-T-G

128610067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127580106-G-A

128610133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127580129-G-A

128610297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127580287-A-G

128610456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127580397-G-A

128610611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127580787-T-C

128610639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127580815-T-C

128615987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127581755-A-G

128615999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127581768-G-A

128616009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127581778-C-G

128616013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127581782-G-A

128616013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127581782-G-C

128616013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127581782-G-T

http://identifiers.org/hco/12/GRCh38#128616047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127581803-C-A

128616047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127581803-C-T

128616102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127581875-G-A

128616102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127581875-G-C

128616102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127581875-G-T

128616345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127582119-G-C

128616446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127582180-T-C

128616448-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127582182-T-G

http://identifiers.org/hco/12/GRCh38#128616452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127582186-A-C

http://identifiers.org/hco/12/GRCh38#128616471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127582205-C-A

128616476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127582210-G-T

128616925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127583167-T-C

128617140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127583308-G-C

128617141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127583309-G-A

128617141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127583309-G-T

128617290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127583406-G-C

128618084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127584397-A-T

128618201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127584519-C-T

128618344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127584656-T-A

128618344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127584656-T-C

128619340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127585977-G-A

http://identifiers.org/hco/12/GRCh38#128620555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127586788-A-C

http://identifiers.org/hco/12/GRCh38#128620640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127586873-C-A

128620640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127586873-C-T

128620684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127586910-G-T

128620725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127586948-C-T

128620876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127587081-G-A

128620890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127587093-G-A

128620890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127587093-G-C

128620890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127587093-G-T

128634875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127589515-A-G

128634903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127589544-G-A

128634981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127589684-G-A

128634987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127589690-G-A

128635012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127589701-T-C

128635146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127589818-A-G

128635453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127590101-G-T

128635469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127590117-T-C

128635578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127590221-A-G

128635645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127590288-G-T

http://identifiers.org/hco/12/GRCh38#128635657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127590299-C-A

128635657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127590299-C-G

128635668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127590310-C-G

128635684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127590315-A-T

128635721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127590352-G-A

http://identifiers.org/hco/12/GRCh38#128635773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127590402-C-A

128635773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127590402-C-T

128637768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127593218-C-G

128638072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127593489-G-C

128638141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127593557-T-C

128638185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127593592-C-T

128638238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127593667-G-A

http://identifiers.org/hco/12/GRCh38#128638351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127593798-A-C

128638368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127593818-A-G

128639406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127593994-A-G

128639620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127594402-T-C

128639782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127594544-G-A

128639783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127594545-A-G

128639853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127594617-A-G

128640074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127594920-C-T

128640095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127594941-G-A

128640095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127594941-G-C

http://identifiers.org/hco/12/GRCh38#128640114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127594960-A-C

http://identifiers.org/hco/12/GRCh38#128640298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127595149-A-C

128640519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127595323-G-A

128640519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127595323-G-T

128641324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127595959-G-A

128641408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127596040-G-A

128641408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127596040-G-T

128641644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127596246-G-A

128641655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127596254-A-G

128642997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127598345-C-T

128643020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127598361-C-G

128643020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127598361-C-T

128643028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127598369-C-T

128643320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127598671-C-T

128643326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127598677-C-T

128649902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127602479-G-A

128650014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127602595-G-C

128650123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127602704-G-A

128650123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127602704-G-T

128650191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127602773-G-A

128650847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127603299-C-T

128652186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127605148-T-G

128652231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127605191-G-A

128652426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127605433-T-C

128652536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127605545-A-G

128652552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127605561-A-G

128652705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127605710-C-T

128652843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127605843-G-A

128652843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127605843-G-C

128652861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127605864-G-A

128652861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127605864-G-T

128652866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127605869-G-A

128666350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127610914-C-T

128666450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127611009-C-T

http://identifiers.org/hco/12/GRCh38#128666454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127611013-C-A

128666483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127611034-G-A

128666621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127611155-C-T

128666769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127611313-G-A

128666817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127611353-A-T

128667077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127611421-A-G

128667249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127611535-C-T

128667358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127611635-C-T

128667382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127611651-C-G

128667438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127611707-G-C

http://identifiers.org/hco/12/GRCh38#128667571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127611837-C-A

128667571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127611837-C-T

128667943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127612160-G-C

128669018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127613118-A-G

128669341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127613350-T-C

128669341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127613350-T-G

http://identifiers.org/hco/12/GRCh38#128669357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127613365-C-A

128669357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127613365-C-T

128669379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127613386-A-G

128669393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127613400-A-G

128669434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127613439-C-T

http://identifiers.org/hco/12/GRCh38#128669482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127613487-C-A

128669485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127613490-T-C

128669491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127613496-G-A

128669545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: missense variant
orthologous variants: 127613550-C-G

128669545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: synonymous variant
orthologous variants: 127613550-C-T

128672334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127614030-C-T

http://identifiers.org/hco/12/GRCh38#128672541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#127614248-C-A

128672636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127614346-G-A

128672688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127614426-G-A

128672739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127614529-G-A

128672820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127614615-A-G

128672876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127614672-G-A

128673025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127614808-T-G

128673106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25436
most severe consequence: intron variant
orthologous variants: 127614889-T-C