11841423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111622219-A-G

http://identifiers.org/hco/11/GRCh38#11841437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111622233-C-A

11841437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111622233-C-T

11841493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111622248-A-G

11841493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111622248-A-T

11841567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111622325-T-C

11841588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111622346-G-A

11841604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111622353-A-G

11841610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111622361-G-A

11841610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111622361-G-T

11841795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111622507-C-G

11841796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111622508-T-C

11841880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 111622601-G-A

11841880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 111622601-G-C

http://identifiers.org/hco/11/GRCh38#11841904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111622625-C-A

11841904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5 prime UTR variant
orthologous variants: 111622625-C-G

11841904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5 prime UTR variant
orthologous variants: 111622625-C-T

11841993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111622719-G-A

11841993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111622719-G-C

11841993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111622719-G-T

http://identifiers.org/hco/11/GRCh38#11841995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#111622721-C-A

11841995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111622721-C-T

11842019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 111622745-T-G

http://identifiers.org/hco/11/GRCh38#11842655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111623372-C-A

11842802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111623556-G-A

11843326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111624076-G-A

11843367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111624288-A-G

11843628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111624530-T-G

11843666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111624564-T-C

11843696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111624595-C-T

11843830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111624722-T-A

11843830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111624722-T-G

11843840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111624732-G-T

11843978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111624837-C-G

11844043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111624911-T-A

11844171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111625049-T-C

11844451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111625208-C-T

11844564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111625311-A-G

11844618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111625356-G-A

11844704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111625444-T-G

11845233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111625865-G-A

11845488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111626104-G-A

11846131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111626683-T-C

11846394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111626900-A-G

http://identifiers.org/hco/11/GRCh38#11846616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111627208-A-C

11846954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111627495-G-A

11846954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111627495-G-T

http://identifiers.org/hco/11/GRCh38#11846959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111627500-C-A

http://identifiers.org/hco/11/GRCh38#11846966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111627507-A-C

11847279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111627740-G-T

11847680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111627964-G-C

11850320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111629204-C-T

11850330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111629214-G-T

11850453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111629370-A-T

11851116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111630178-T-A

11851337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111630361-G-T

http://identifiers.org/hco/11/GRCh38#11851448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111630448-A-C

11851448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111630448-A-T

11851701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111630679-A-G

11851701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111630679-A-T

11851865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111630842-G-A

11852767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111631761-T-C

11852791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111631785-C-T

11853113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111632117-A-T

11853127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111632131-T-A

11853324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111632306-G-A

11853507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111632498-A-G

11853538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111632536-A-G

11854263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111632669-C-G

11854452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111632814-G-A

11855684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111634927-C-G

11856055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111635299-C-T

11856137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111635399-C-G

11856137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111635399-C-T

11856324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111635579-A-G

11856366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111635617-A-G

11856459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111635702-T-C

http://identifiers.org/hco/11/GRCh38#11856612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111635844-C-A

11856612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111635844-C-T

11856629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111635869-A-G

http://identifiers.org/hco/11/GRCh38#11856639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111635879-C-A

11856758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111636000-A-G

11856793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111636035-T-A

11856793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111636035-T-C

http://identifiers.org/hco/11/GRCh38#11856805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#111636045-C-A

11856805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111636045-C-T

11856808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111636048-T-C

11856982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111636696-G-T

11857004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111636718-A-G

11857128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111636826-G-A

11857466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111637137-A-G

http://identifiers.org/hco/11/GRCh38#11858492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111637402-A-C

11858910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111637851-A-G

11859121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111638053-A-G

http://identifiers.org/hco/11/GRCh38#11859126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111638060-A-C

11859383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111638286-A-G

11859665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111638688-T-C

11860747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111639751-G-A

11861538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111640096-C-T

11861763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111640266-A-G

11861848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111640348-A-G

11872077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111644763-G-A

11872199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111644861-C-T

11872618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111645220-T-A

11872959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111645509-T-C

11873032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111645575-A-G

11873889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111646223-G-A

11873889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111646223-G-T

11874058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111646393-G-A

11874134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111646456-T-C

11874244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111646765-A-G

11875957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111648244-G-T

11875973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111648258-G-A

11876041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111648298-C-T

11876050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111648307-G-A

11876209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111648438-G-A

http://identifiers.org/hco/11/GRCh38#11876274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111648497-A-C

11876274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111648497-A-T

11876681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111648855-G-T

11876757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111648926-C-T

11876812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111648976-G-A

11876963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111649100-G-A

11876967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111649104-T-C

11877322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111649411-G-A

11877410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111649504-G-A

11877897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111650081-A-G

http://identifiers.org/hco/11/GRCh38#11878452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111650655-A-C

11878452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111650655-A-G

11878546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111650746-A-G

11878624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 111650830-A-G

11878630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111650836-A-G

11878876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111651104-G-A

11879621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111651936-C-T

http://identifiers.org/hco/11/GRCh38#11880090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111652348-C-A

11880090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111652348-C-G

11880090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111652348-C-T

11880439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111652702-C-T

11880509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111652761-A-G

11880509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111652761-A-T

11881092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111653143-T-G

11881209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111653249-G-A

11881209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111653249-G-C

11881209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111653249-G-T

11881309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111653316-C-G

11881309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111653316-C-T

http://identifiers.org/hco/11/GRCh38#11881428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111653418-A-C

11884219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111653812-G-A

11884260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111653853-G-A

11884392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111653976-G-A

11884413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111653997-G-A

11884413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111653997-G-C

11884413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111653997-G-T

http://identifiers.org/hco/11/GRCh38#11884654-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111654214-A-C

11884654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111654214-A-G

11884687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 111654242-A-G

11884791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111654313-G-A

11884791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111654313-G-T

11884826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111654323-G-A

11884826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111654323-G-T

11891345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111655093-A-G

11891351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111655099-C-T

11891372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111655117-C-G

11891384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111655129-A-G

11891525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111655248-T-C

11891564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111655286-C-T

11891634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111655355-G-A

11891947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111655661-T-C

11891947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111655661-T-G

11892046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, missense_variant
orthologous variants: 111655760-A-G

11892191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111655897-A-G

11892191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111655897-A-T

11892224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111655928-A-G

11893350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111656897-C-G

11893869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111656994-G-A

11894559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111657338-C-T

11894913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111657646-C-T

11897313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111657920-A-G

11897353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111657964-T-A

11897353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111657964-T-C

11897468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111658069-G-T

11897714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111658297-T-A

11897730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111658308-T-C

11898651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111659302-A-G

11898718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111659377-G-C

11899086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111659752-C-G

11899132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111659799-A-G

11899137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111659804-C-T

11899313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111659929-G-A

11899588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111660183-T-C

11900482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111660450-G-T

11900602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111660560-G-A

11900609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111660566-T-C

11900625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111660582-G-A

11901459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111661193-G-C

11902058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111661863-T-C

http://identifiers.org/hco/11/GRCh38#11902067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111661873-C-A

11902911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111662647-G-T

http://identifiers.org/hco/11/GRCh38#11902938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111662662-C-A

11902938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111662662-C-T

11902967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111662698-A-G

11903674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111664387-G-A

11904452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111665244-A-T

11905366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111666259-G-A

11905366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111666259-G-C

11905366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111666259-G-T

11905380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111666273-G-A

http://identifiers.org/hco/11/GRCh38#11905443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/7/GRCm39#111666336-C-A

11905443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 111666336-C-T

http://identifiers.org/hco/11/GRCh38#11905564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111666457-C-A

11905564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111666457-C-G

11905564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111666457-C-T

11905576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111666463-G-A

11905576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111666463-G-T

11908928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 111667461-T-C

11920164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 111673687-A-G

11920245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 111673768-A-G

11920719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111674457-G-A

11921328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111675078-A-G

11921679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111675920-G-A

11921927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111676247-G-C

11922159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111676479-A-T

11922258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111676562-A-G

11922309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111676605-C-T

11922670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111676945-G-T

11922919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111677192-T-A

11922919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111677192-T-C

11922923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111677196-A-G

11923006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111677317-G-A

11923006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111677317-G-T

11923009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111677320-A-G

11923418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111677600-G-A

11927906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111678287-A-G

11927938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111678322-T-C

11927938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111678322-T-G

11928333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111678663-A-G

11928702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111680470-G-C

11928702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111680470-G-T

11929253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111681473-T-C

11929355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111681564-G-A

11929886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111682013-C-T

11929923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111682038-G-T

http://identifiers.org/hco/11/GRCh38#11929969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111682084-A-C

11929981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111682224-A-G

11929981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111682224-A-T

11930221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111682469-A-T

11930254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111682494-A-G

11930288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111682574-A-G

http://identifiers.org/hco/11/GRCh38#11931115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111684113-A-C

11931115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111684113-A-G

11932934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111685145-A-T

11933074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: missense variant
orthologous variants: 111685272-A-T

http://identifiers.org/hco/11/GRCh38#11933186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111685369-A-C

http://identifiers.org/hco/11/GRCh38#11933224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111685406-C-A

11933224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111685406-C-T

11933236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111685416-A-T

http://identifiers.org/hco/11/GRCh38#11933258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111685434-A-C

11933258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111685434-A-G

11933258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111685434-A-T

11933587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111685959-T-C

11933730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111686102-T-C

11933787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111686158-A-G

11934094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111686428-G-C

11937838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111688207-A-G

11938156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron variant
orthologous variants: 111688584-G-T

11938378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111688853-T-C

11938683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111689129-C-T

11938691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111689136-A-G

11938785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111689250-G-A

11939064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111689662-G-A

11939099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111689697-G-C

11939222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111689813-G-A

11939227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111689818-A-G

11939337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111689895-C-T

11939376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111689934-C-T

11940574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111690756-A-G

11940834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111690975-G-T

11942228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111691809-G-A

11942228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111691809-G-T

http://identifiers.org/hco/11/GRCh38#11942829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111692410-A-C

11942829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 111692410-A-G

11943211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111692783-T-C

11943213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111692785-A-G

http://identifiers.org/hco/11/GRCh38#11943225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111692792-C-A

11943225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111692792-C-T

11943243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111692810-G-A

11943243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111692810-G-T

http://identifiers.org/hco/11/GRCh38#11943361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111692897-A-C

11943361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111692897-A-T

11943619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111693534-G-A

http://identifiers.org/hco/11/GRCh38#11943630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111693548-C-A

11946604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111699480-T-C

11946772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111699636-G-A

11946772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111699636-G-T

11947074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111699895-G-T

11947116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111699957-C-T

11947325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111700251-C-G

11947378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111700297-C-T

11947576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111700472-G-A

11947599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111700482-G-A

11947717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111700693-A-G

http://identifiers.org/hco/11/GRCh38#11947813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111700813-A-C

11947859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111700863-A-G

11948135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111701135-T-C

11948165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111701161-A-G

http://identifiers.org/hco/11/GRCh38#11948189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111701213-A-C

11948189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111701213-A-G

11948223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111701371-G-T

http://identifiers.org/hco/11/GRCh38#11948369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111701537-C-A

11948369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111701537-C-G

11948369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111701537-C-T

11948385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111701553-T-C

11948779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111702144-T-A

http://identifiers.org/hco/11/GRCh38#11949001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111702428-C-A

11949001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111702428-C-T

11949144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702569-T-G

11949175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111702598-G-T

11949739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111703020-G-T

11950261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111703458-G-A

11950261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111703458-G-C

11950261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111703458-G-T

11950337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111703530-G-A

11950337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111703530-G-T

11950541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111703733-G-A

11950541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111703733-G-T

11951076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111704202-G-T

11951092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111704231-T-C

http://identifiers.org/hco/11/GRCh38#11951101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111704237-C-A

http://identifiers.org/hco/11/GRCh38#11951160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111704309-C-A

11951160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111704309-C-T

11951190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111704338-G-A

11951190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111704338-G-T

http://identifiers.org/hco/11/GRCh38#11951382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111704510-C-A

11951645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111704687-A-T

11951732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111704762-G-C

11951732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111704762-G-T

11951754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111704784-C-T

11952452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111705344-A-G

11952504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111705438-G-T

11952505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111705439-A-G

11952505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111705439-A-T

http://identifiers.org/hco/11/GRCh38#11952514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111705448-A-C

11952522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111705456-T-G

11952687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111705932-A-T

11952876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706121-G-A

http://identifiers.org/hco/11/GRCh38#11952879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111706124-C-A

11953017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706186-C-G

11953017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706186-C-T

11953019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706188-T-C

11953348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706591-T-C

11953348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111706591-T-G

11954807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707559-G-A

11954807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707559-G-T

11954855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707605-T-A

11954882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707629-T-G

11954964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707710-G-T

11954965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707711-C-T

11955016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111707763-C-T

11955290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111708004-G-A

11955290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111708004-G-T

11955389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111708652-A-G

11955636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111708847-T-A

11955745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111708933-A-G

11955921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111709077-A-G

http://identifiers.org/hco/11/GRCh38#11955943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111709099-C-A

11955943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111709099-C-G

11955943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111709099-C-T

11955959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111709114-G-A

11956002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 111709153-G-A

11956019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 111709170-A-G

11956390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111709534-G-T

http://identifiers.org/hco/11/GRCh38#11956581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111709702-A-C

11956885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111709993-G-T

11956949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111710063-C-T

11957610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111710687-T-C

http://identifiers.org/hco/11/GRCh38#11958053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111710877-C-A

11958105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111710919-T-G

http://identifiers.org/hco/11/GRCh38#11958126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111710940-C-A

11958126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111710940-C-T

11958257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711064-C-T

11958259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711066-G-A

11958355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711142-A-T

11958403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711189-G-A

11958540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711277-G-T

11958567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711303-T-C

http://identifiers.org/hco/11/GRCh38#11958596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111711330-C-A

11958596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711330-C-T

11958718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711443-G-T

11958724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711449-G-T

11958751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711473-G-C

11958751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711473-G-T

11958756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711478-G-T

http://identifiers.org/hco/11/GRCh38#11958781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111711503-C-A

11958781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711503-C-T

11958938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711668-A-G

11959078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711783-G-T

11959121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711811-T-C

http://identifiers.org/hco/11/GRCh38#11959169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111711862-C-A

11959169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3 prime UTR variant
orthologous variants: 111711862-C-T

11959196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3 prime UTR variant
orthologous variants: 111711889-C-T

11959291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3 prime UTR variant
orthologous variants: 111711958-T-C

11959384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3 prime UTR variant
orthologous variants: 111712050-A-G

11959390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3 prime UTR variant
orthologous variants: 111712056-C-G

11959519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20076
most severe consequence: 3 prime UTR variant
orthologous variants: 111712154-A-G