11691321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148215526-G-A

11691321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148215526-G-T

http://identifiers.org/hco/1/GRCh38#11691327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#148215509-C-A

11691327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148215509-C-G

11691327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148215509-C-T

11691329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148215507-C-T

11691333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148215503-G-A

11691409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148215425-G-A

11691409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148215425-G-T

11691456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 148215378-G-A

11691456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 148215378-G-T

11691533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 148215304-T-C

11691534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 148215303-G-T

11691542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 148215295-A-G

11691627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148215207-G-A

11691627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148215207-G-T

http://identifiers.org/hco/1/GRCh38#11691635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148215205-C-A

11691635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148215205-C-T

http://identifiers.org/hco/1/GRCh38#11691636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148215204-C-A

11691636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148215204-C-T

11691663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148215177-G-A

11691663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148215177-G-C

http://identifiers.org/hco/1/GRCh38#11691722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148215137-C-A

11691722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148215137-C-T

http://identifiers.org/hco/1/GRCh38#11691729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148215132-A-C

11691729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148215132-A-G

11691742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148215119-G-A

11691742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 148215119-G-T

11691750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 148215111-A-G

http://identifiers.org/hco/1/GRCh38#11691866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148215011-C-A

11691866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148215011-C-T

http://identifiers.org/hco/1/GRCh38#11691878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148214999-C-A

11691921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148214959-A-G

http://identifiers.org/hco/1/GRCh38#11692005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148214908-C-A

11692026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148214887-C-G

11692267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148214653-A-T

http://identifiers.org/hco/1/GRCh38#11692444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148214493-C-A

11692485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148214475-G-A

11692510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148214452-C-G

11692535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148214427-C-T

11692537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148214425-G-A

11692683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148214260-G-A

11692697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148214246-C-T

11692957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148214020-G-A

11693004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148213973-C-T

11693539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148213524-T-C

11693710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148213388-T-C

http://identifiers.org/hco/1/GRCh38#11693823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148213270-C-A

11694342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148212765-G-A

11694396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148212708-C-T

11694507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148212621-T-C

11694802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148212349-G-A

11694864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148212297-C-G

11695148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148212046-G-A

11695299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148211903-C-T

11695931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148211404-C-T

11695940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148211395-T-C

11695955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148211384-G-T

11695956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148211383-T-C

11696005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148211331-A-G

http://identifiers.org/hco/1/GRCh38#11696150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148211204-C-A

11700996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148206917-C-T

http://identifiers.org/hco/1/GRCh38#11701927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148205947-C-A

11702062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148205849-A-G

11703986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148203425-A-T

11705033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148203106-G-A

11705033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148203106-G-T

http://identifiers.org/hco/1/GRCh38#11705163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148203013-C-A

11705163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148203013-C-G

11705286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148202920-C-T

11705369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148202815-T-C

11705587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148202426-T-C

11705869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148202225-T-C

11705873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148202221-G-A

http://identifiers.org/hco/1/GRCh38#11706193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148200513-A-C

11706193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148200513-A-G

11706193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148200513-A-T

11706195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148200511-G-A

11706195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148200511-G-C

11706195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148200511-G-T

11706203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148200503-G-C

11706203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148200503-G-T

11706205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148200501-G-A

11706205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148200501-G-T

11706214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148200495-G-A

11706214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148200495-G-T

11706244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 148200460-T-A

11706244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 148200460-T-G

11706315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: synonymous variant
orthologous variants: 148200390-C-G

11706639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: synonymous variant
orthologous variants: 148200084-A-T

11706696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: synonymous variant
orthologous variants: 148200027-G-A

11706731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148199992-G-A

11706731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148199992-G-T

11706795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148199879-G-A

11706795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148199879-G-C

11706795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148199879-G-T

11706856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148199813-A-G

11706856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148199813-A-T

11706861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148199808-G-A

11706861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148199808-G-T

11707972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 148198463-A-G

11708325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 148198155-G-A

11708634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148197943-C-T

11708788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148197772-G-A

11708815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148197754-G-A

11708912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148197669-C-T

11708984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148197624-C-T

11709021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148197587-G-A

11709061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148197551-A-G

11709149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148197495-G-A

11709149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148197495-G-T

11709174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148197475-C-T

http://identifiers.org/hco/1/GRCh38#11709226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148197401-C-A

11709226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148197401-C-G

11709226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148197401-C-T

11709228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148197399-A-G

11709239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148197388-A-G

11709407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: missense variant
orthologous variants: 148197225-A-T

11709498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148197136-A-G

11709509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148197125-G-T

11709516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148197122-T-C

11711188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148195113-T-A

http://identifiers.org/hco/1/GRCh38#11711275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148195023-C-A

11711311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148194969-C-T

11711325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148194959-T-C

11711869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: missense variant
orthologous variants: 148194596-G-A

11712030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148194441-G-A

11712036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148194435-G-A

11712104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148194378-G-T

http://identifiers.org/hco/1/GRCh38#11712225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148194256-C-A

http://identifiers.org/hco/1/GRCh38#11712235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148194246-C-A

11712235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148194246-C-T

http://identifiers.org/hco/1/GRCh38#11712236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148194245-C-A

11712236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148194245-C-T

11712239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148194242-G-T

11712496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148193992-G-C

11712496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148193992-G-T

11712515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148193987-A-G

11712518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148193984-T-C

http://identifiers.org/hco/1/GRCh38#11712555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148193947-C-A

11712555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148193947-C-T

11714525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148193085-G-A

http://identifiers.org/hco/1/GRCh38#11715043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#148192561-C-A

11715043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148192561-C-G

11715043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148192561-C-T

http://identifiers.org/hco/1/GRCh38#11715053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148192551-C-A

11715053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148192551-C-G

11715053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148192551-C-T

11715063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148192543-G-A

11715063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148192543-G-T

11715092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148192506-G-A

11715187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: missense variant
orthologous variants: 148192411-G-A

11715187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: missense variant
orthologous variants: 148192411-G-T

11715214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148192384-T-A

11715214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148192384-T-C

11715253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148192333-C-G

11715488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148192093-C-T

11719127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron variant
orthologous variants: 148187466-C-T

11719529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148187090-A-G

11719539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148187080-A-G

11719542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148187077-G-T

http://identifiers.org/hco/1/GRCh38#11719560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#148187060-C-A

11719560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148187060-C-T

http://identifiers.org/hco/1/GRCh38#11719562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#148187058-C-A

11719568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: intron_variant, undefined
orthologous variants: 148187053-G-T

11719628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: missense variant
orthologous variants: 148186993-C-G

http://identifiers.org/hco/1/GRCh38#11719631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148186990-A-C

11719652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: missense variant
orthologous variants: 148186969-C-T

11719696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: undefined
orthologous variants: 148186925-G-A

11719704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148186904-G-A

11719713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148186895-G-C

11719713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148186895-G-T

11719743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148186864-G-A

11719743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148186864-G-T

http://identifiers.org/hco/1/GRCh38#11719810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148186799-A-C

11719810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148186799-A-G

11719810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148186799-A-T

http://identifiers.org/hco/1/GRCh38#11719834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148186774-A-C

11719877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148186738-C-T

http://identifiers.org/hco/1/GRCh38#11719927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#148186701-C-A

11719927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148186701-C-T

11719933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148186695-G-T

11720005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148186619-T-C

11720194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148186477-A-T

11720220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148186450-T-A

11720220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148186450-T-C

11720236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148186436-A-G

11720497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148186175-G-A

11720497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148186175-G-T

11720519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148186151-G-A

11720519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148186151-G-T

11720639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148186069-G-T

http://identifiers.org/hco/1/GRCh38#11720687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148186060-C-A

11720974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185959-T-C

http://identifiers.org/hco/1/GRCh38#11721071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148185848-C-A

http://identifiers.org/hco/1/GRCh38#11721097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148185837-C-A

11721097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185837-C-T

http://identifiers.org/hco/1/GRCh38#11721156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148185778-C-A

11721156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185778-C-T

11721162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185772-T-C

11721282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185662-T-C

11721391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185571-C-T

11721404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185558-T-C

11721456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185527-A-G

11721630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185353-G-A

11721640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185347-G-T

11721647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185340-A-G

http://identifiers.org/hco/1/GRCh38#11721649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148185338-C-A

11721649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185338-C-T

11721657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185330-G-A

11721657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185330-G-T

http://identifiers.org/hco/1/GRCh38#11721658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148185329-C-A

11721658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185329-C-T

11721659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185328-A-G

11721659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185328-A-T

11721660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185327-G-A

11721660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185327-G-T

http://identifiers.org/hco/1/GRCh38#11721676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148185311-A-C

11721676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148185311-A-G

11724173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148184470-G-A

11724173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148184470-G-T

http://identifiers.org/hco/1/GRCh38#11724186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148184457-C-A

11724290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148184362-C-G

11724295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148184357-G-A

11724349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148184324-G-A

11724379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148184294-G-A

11724379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148184294-G-T

http://identifiers.org/hco/1/GRCh38#11724464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148184205-C-A

11724464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148184205-C-T

http://identifiers.org/hco/1/GRCh38#11724568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148184115-C-A

11724674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148184055-C-T

11724707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148184022-G-A

11724747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183984-T-A

11724750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183981-T-C

11724763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183974-G-C

11724763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183974-G-T

11724859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183876-A-G

11724956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183770-C-T

11725022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183708-A-G

11725106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183681-A-G

11725116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183661-T-C

11725121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183656-G-A

11725125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183652-A-G

11725368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183546-C-T

11725396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183519-G-A

11725396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183519-G-T

11725397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183518-G-T

11725508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183403-G-A

11725531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183376-G-A

http://identifiers.org/hco/1/GRCh38#11725608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#148183298-C-A

11725678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183068-C-T

11725682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183064-C-T

11725685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183061-G-T

11725693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183053-A-G

11725700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148183046-G-T

11725746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148182997-T-C

11725752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148182991-T-C

11725761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148182982-G-A

11725761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148182982-G-T

11725769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148182974-G-T

11725782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148182965-C-G

11725782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148182965-C-T

11725783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148182964-A-G

11725783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 148182964-A-T

11725824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148182926-G-A

11725824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25054
most severe consequence: 3 prime UTR variant
orthologous variants: 148182926-G-T