24056256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135542644-C-T

24056307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135542598-T-C

24056344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135542561-T-C

24056679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135542481-T-C

24056736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135542434-C-T

24056757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135542413-A-G

http://identifiers.org/hco/1/GRCh38#24056931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135542263-C-A

24056931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135542263-C-G

24056931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135542263-C-T

http://identifiers.org/hco/1/GRCh38#24057157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135541918-C-A

24057157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135541918-C-G

24057157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135541918-C-T

24057187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135541888-A-G

24057187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135541888-A-T

http://identifiers.org/hco/1/GRCh38#24057194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135541881-C-A

24057194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135541881-C-T

http://identifiers.org/hco/1/GRCh38#24057274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135541813-C-A

24057274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135541813-C-T

http://identifiers.org/hco/1/GRCh38#24057350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135541741-C-A

24057350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135541741-C-T

24057353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135541738-G-A

24057353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 135541738-G-C

24057377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135541715-A-G

24057377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135541715-A-T

http://identifiers.org/hco/1/GRCh38#24057407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135541685-A-C

24057503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135541589-A-G

24057563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135541529-T-C

24057599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135541493-C-T

http://identifiers.org/hco/1/GRCh38#24057616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135541476-C-A

24058347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135540355-A-T

24058349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135540353-G-C

24058806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135539955-G-T

24058858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135539875-T-A

http://identifiers.org/hco/1/GRCh38#24058859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135539874-C-A

24058867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135539866-G-T

24058868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135539865-A-G

http://identifiers.org/hco/1/GRCh38#24058946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135539786-A-C

24059568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135539530-A-G

24059621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135539479-A-G

http://identifiers.org/hco/1/GRCh38#24059763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135539374-A-C

24059855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135539298-G-A

24060014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135539149-A-G

24060236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538957-C-G

24060236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538957-C-T

24060325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538892-C-T

24060431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538815-T-C

24060431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538815-T-G

24060713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538555-C-T

24060800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538466-C-T

24060806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538460-T-C

24060815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538451-C-T

24060837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538429-G-T

http://identifiers.org/hco/1/GRCh38#24060838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135538428-C-A

24060838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538428-C-T

24060869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538411-A-G

24060870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538410-A-G

24060899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538385-C-T

24060951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538363-A-G

24061263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538104-G-A

24061276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135538091-A-G

24061285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135538082-T-C

24061360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538033-A-G

24061360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538033-A-T

http://identifiers.org/hco/1/GRCh38#24061422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135538001-C-A

24061422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135538001-C-T

24061426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135537997-G-T

24061925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135536301-A-G

24062014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135536200-C-T

http://identifiers.org/hco/1/GRCh38#24062174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135536043-C-A

24062214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135536031-A-G

24062214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135536031-A-T

http://identifiers.org/hco/1/GRCh38#24062247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135535998-C-A

24062419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135535194-C-G

24062419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135535194-C-T

24062458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135535157-A-G

24062557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135535064-G-A

24062567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135535054-T-C

24062858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534793-T-C

24062954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534734-C-G

24062954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534734-C-T

24062980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534710-T-C

24063069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534642-G-A

24063069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534642-G-C

24063069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534642-G-T

24063097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534615-G-A

24063097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534615-G-C

24063097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534615-G-T

24063138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135534574-G-A

24063156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135534556-A-G

24063237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135534475-G-A

24063242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135534470-G-A

24063242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135534470-G-T

24063313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534406-T-C

24063363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534362-G-A

24063363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534362-G-T

24063364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534361-G-C

24063364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534361-G-T

24063460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534268-G-A

24063517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135534206-G-A

24063555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534173-T-G

24063582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534148-G-A

24063583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534147-T-C

http://identifiers.org/hco/1/GRCh38#24063633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135534098-C-A

24063633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135534098-C-T

24063872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135533630-G-A

24063929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135533589-A-G

24063975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135533543-G-A

24063975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135533543-G-T

24063987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135533531-T-C

24064003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135533515-G-A

24064003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135533515-G-C

24064003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135533515-G-T

24064063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135533443-A-G

http://identifiers.org/hco/1/GRCh38#24064190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135533329-A-C

24064191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135533328-G-A

24064191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135533328-G-T

24064218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135533310-A-G

24064218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135533310-A-T

24064265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135533274-T-A

24064265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135533274-T-C

24064267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135533272-A-G

24064505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135532500-G-T

24064526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135532467-C-T

24064837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135532073-A-G

24065162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135531733-G-C

24065336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135531599-G-A

24065415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135531531-C-G

24065478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135531489-C-T

http://identifiers.org/hco/1/GRCh38#24065564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135531444-C-A

24065564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135531444-C-T

24065675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135531325-A-G

http://identifiers.org/hco/1/GRCh38#24065801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135530712-C-A

24065801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135530712-C-T

24065994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135530524-T-C

24065994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135530524-T-G

24066011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135530507-G-C

24066011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135530507-G-T

24066031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135530487-G-C

24066031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135530487-G-T

24066050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135530470-G-C

http://identifiers.org/hco/1/GRCh38#24066087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135530395-A-C

24066087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135530395-A-G

24066112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135530370-G-A

24066112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135530370-G-C

24066112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135530370-G-T

24066160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135530339-C-G

24066160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135530339-C-T

http://identifiers.org/hco/1/GRCh38#24066289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135530207-C-A

http://identifiers.org/hco/1/GRCh38#24066912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135529207-C-A

24066912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135529207-C-T

http://identifiers.org/hco/1/GRCh38#24067027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135529086-C-A

24067027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135529086-C-G

24067027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135529086-C-T

http://identifiers.org/hco/1/GRCh38#24067094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135529019-C-A

24067094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135529019-C-T

24067137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528975-C-G

24067167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528936-G-A

24067167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528936-G-C

24067167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528936-G-T

24067199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528906-C-G

24067231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528880-G-A

24067231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528880-G-T

24068143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528550-G-T

24068156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528537-A-T

24068205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528473-A-G

24068342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135528336-T-A

24068342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135528336-T-C

24068372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135528307-A-G

24068435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528237-G-A

24068436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528236-T-G

24068437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528235-G-A

24068450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528222-G-A

24068450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528222-G-T

24068459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528213-G-A

24068459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528213-G-T

24068476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528196-T-A

http://identifiers.org/hco/1/GRCh38#24068504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135528168-A-C

24068504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528168-A-G

24068504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528168-A-T

http://identifiers.org/hco/1/GRCh38#24068518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135528137-C-A

24068518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135528137-C-T

24070785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135526019-G-T

24070957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135525877-A-G

24070988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135525851-A-G

24070995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135525844-G-A

24070995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135525844-G-T

24070999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135525841-A-G

24070999-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135525841-A-T

24071036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135525804-A-G

24071081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135525773-G-A

24071081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135525773-G-C

24071082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135525772-G-T

24071127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 135525730-A-G

24071163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135525694-G-C

24071175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135525682-A-G

24071193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135525664-C-G

24071196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135525661-A-G

24071356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135525446-A-G

http://identifiers.org/hco/1/GRCh38#24071394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135525414-C-A

24071780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524970-C-G

24071861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524906-C-T

24071864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524903-T-G

24071883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524880-C-T

24072014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 135524762-C-G

24072022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524754-G-A

http://identifiers.org/hco/1/GRCh38#24072045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135524731-A-C

24072071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524709-T-C

24072071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524709-T-G

24072126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524663-A-T

http://identifiers.org/hco/1/GRCh38#24072149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135524635-C-A

24072149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524635-C-T

http://identifiers.org/hco/1/GRCh38#24072191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135524609-C-A

24072215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524585-G-A

24072230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524570-C-T

24072233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524567-C-T

24072251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524549-C-G

24072350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524484-G-A

24072399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524439-A-G

24074140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524397-G-T

24074165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135524377-T-C

24074296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135524247-C-G

24075184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135523901-A-T

24075218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135523867-G-T

http://identifiers.org/hco/1/GRCh38#24075230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135523849-C-A

24075230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135523849-C-T

http://identifiers.org/hco/1/GRCh38#24075239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135523832-C-A

24075287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135523768-T-G

24075305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135523760-C-T

24075311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135523754-T-C

http://identifiers.org/hco/1/GRCh38#24075801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135523084-A-C

24075801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135523084-A-G

24075976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522917-T-C

24076014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522737-A-G

24076026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522665-G-A

24076033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522631-G-A

24076033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522631-G-T

24076036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522628-G-A

24076036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522628-G-T

24076057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522603-G-C

24076057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522603-G-T

24076114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522545-G-T

24076191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135522473-G-A

24076191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135522473-G-T

24076323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522353-T-C

http://identifiers.org/hco/1/GRCh38#24076329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135522347-C-A

24076329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522347-C-G

24076329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522347-C-T

24076522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522134-T-C

24076522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522134-T-G

24076599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522072-C-T

24076617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135522054-C-G

24076809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135521866-C-T

24076916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135521766-G-A

http://identifiers.org/hco/1/GRCh38#24077125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135520889-C-A

24077222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135520794-C-T

24077223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135520793-T-C

24077529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135520517-G-A

24077689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135520358-C-G

24077691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135520356-T-C

24077700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135520347-A-G

24077704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135520343-G-C

24079059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135517684-T-C

24079104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135517612-G-A

24079122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135517578-T-A

24079167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135517525-A-G

24079649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135517373-C-G

24079653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135517369-C-T

24079741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135517288-G-A

24079748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135517274-G-A

24079898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135517136-T-C

http://identifiers.org/hco/1/GRCh38#24079899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135517135-C-A

24079899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135517135-C-T

24079975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135517043-A-G

24080026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 135517011-G-A

24080298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135516697-T-A

24080298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135516697-T-C

24080325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135516670-T-A

24080325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135516670-T-C

24080335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135516660-G-A

24080335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135516660-G-T

24080565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135516428-T-C

24080576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135516417-G-A

24080695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135516312-T-C

24080723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135516283-A-G

24080758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135516237-T-A

24080919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135516053-G-A

24081230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135515816-G-T

24081259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135515788-T-C

24081274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135515773-A-T

24081303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135515741-T-A

24081480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135515573-A-G

24081480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135515573-A-T

24081485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135515567-G-T

24081693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135515521-G-T

http://identifiers.org/hco/1/GRCh38#24081751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135515502-C-A

24081751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135515502-C-T

http://identifiers.org/hco/1/GRCh38#24081752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135515501-A-C

24081752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant, splice_region_variant
orthologous variants: 135515501-A-G

24081885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135515459-A-T

http://identifiers.org/hco/1/GRCh38#24081992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135515400-C-A

24081992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135515400-C-T

24082073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135515319-C-T

24082248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135515148-G-A

24082248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135515148-G-T

24082250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135515146-G-A

24082250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135515146-G-T

http://identifiers.org/hco/1/GRCh38#24082273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135515131-C-A

24082273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135515131-C-T

http://identifiers.org/hco/1/GRCh38#24082377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135515028-C-A

24082377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135515028-C-T

http://identifiers.org/hco/1/GRCh38#24082408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135514993-C-A

24082408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135514993-C-T

24082446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135514955-A-G

24082446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135514955-A-T

24082481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135514922-G-A

24082510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135514909-G-T

24082559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135514862-G-C

24082559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135514862-G-T

24082622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135514800-G-T

http://identifiers.org/hco/1/GRCh38#24082734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135514688-C-A

24082734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135514688-C-G

24082734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135514688-C-T

24082817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135514618-G-T

24082826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135514609-G-A

24082826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135514609-G-T

24084552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135513213-T-C

24084575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135513187-T-A

24084575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 135513187-T-C

24084666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135513101-G-A

24084786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135512977-A-G

24084894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135512884-T-G

24084910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135512835-C-G

http://identifiers.org/hco/1/GRCh38#24085122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135512442-A-C

24085237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135512335-G-T

24085288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135512281-G-A

24085520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135512139-C-G

http://identifiers.org/hco/1/GRCh38#24085522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135512137-C-A

24085522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135512137-C-T

24085618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135512040-T-A

http://identifiers.org/hco/1/GRCh38#24085651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135512027-C-A

24085670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135512007-G-A

24085671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135512006-C-T

http://identifiers.org/hco/1/GRCh38#24085850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135511173-C-A

24085850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135511173-C-T

24085894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135511137-T-C

24086013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135511041-T-A

24086013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135511041-T-C

24086018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135511036-G-A

24086522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135510622-A-G

http://identifiers.org/hco/1/GRCh38#24086583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135510581-C-A

24086847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135510299-C-T

http://identifiers.org/hco/1/GRCh38#24086909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135510200-C-A

24086909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135510200-C-T

24086992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135510076-T-C

24087029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135510029-C-T

24087042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135510016-G-A

24087042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135510016-G-C

24087081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135509957-C-G

24087400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135509428-T-G

http://identifiers.org/hco/1/GRCh38#24087420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135509408-C-A

24087488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135509327-T-G

24087943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135508897-G-A

24088064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135508780-C-G

24088064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135508780-C-T

http://identifiers.org/hco/1/GRCh38#24088070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135508774-A-C

24088211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135508711-A-G

24088318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135508583-A-G

24088323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135508578-T-A

24088473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135508435-G-A

24088478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135508428-G-A

24088478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135508428-G-T

24088597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135508014-G-A

24088858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135507809-T-C

24088937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135507722-G-T

http://identifiers.org/hco/1/GRCh38#24089009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135507672-C-A

24089009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135507672-C-G

24089081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135507633-G-C

24089232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135507514-C-T

http://identifiers.org/hco/1/GRCh38#24089250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135507496-C-A

24089250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135507496-C-T

http://identifiers.org/hco/1/GRCh38#24089502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135507280-A-C

24089502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135507280-A-G

24089502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135507280-A-T

http://identifiers.org/hco/1/GRCh38#24089556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135507218-C-A

24089556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135507218-C-T

http://identifiers.org/hco/1/GRCh38#24089557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135507217-A-C

24089557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135507217-A-G

24089626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135507148-G-A

24089626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135507148-G-T

http://identifiers.org/hco/1/GRCh38#24089633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135507141-C-A

24089633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135507141-C-T

24089667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 135507107-T-C

24089725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135507039-G-A

24089725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135507039-G-T

24089765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135507005-T-A

24089765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135507005-T-C

24089817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135506953-G-A

24089817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135506953-G-T

24089923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135506843-A-G

http://identifiers.org/hco/1/GRCh38#24089924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135506842-C-A

24089924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135506842-C-T

24089981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135506792-A-G

24089988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135506785-C-T

24090036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135506754-G-A

24090073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135506707-G-A

http://identifiers.org/hco/1/GRCh38#24090213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135506585-C-A

24090213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135506585-C-T

http://identifiers.org/hco/1/GRCh38#24090228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135506572-C-A

24090228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135506572-C-T

http://identifiers.org/hco/1/GRCh38#24090242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135506562-C-A

24090242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135506562-C-T

http://identifiers.org/hco/1/GRCh38#24090245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135506559-C-A

24090245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135506559-C-T

24090416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135506362-C-T

24090750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135505586-T-C

24090805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135505537-C-T

24090808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135505534-C-T

24090886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135505456-C-G

24090907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135505435-T-C

24090969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135505373-G-A

http://identifiers.org/hco/1/GRCh38#24091013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135505330-C-A

24091013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135505330-C-T

24091056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135505296-A-G

24091083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135505272-G-C

24091083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135505272-G-T

24091177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135505212-C-T

24092038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135504439-G-A

24092038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135504439-G-C

24092038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135504439-G-T

http://identifiers.org/hco/1/GRCh38#24092043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135504434-C-A

24092043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135504434-C-T

24092089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503881-A-G

http://identifiers.org/hco/1/GRCh38#24092091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135503879-A-C

24092091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503879-A-G

24092131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503827-A-G

24092134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503824-T-C

24092363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503597-G-T

24092382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503582-T-G

24092398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503568-C-T

24092421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503545-T-A

24092421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503545-T-C

24092438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503528-G-A

24092438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503528-G-T

24092445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503521-G-A

24092445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503521-G-T

24092491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503476-G-A

24092491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135503476-G-C

24092963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135502999-G-C

24092963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135502999-G-T

24092988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135502974-G-T

24093114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135502848-G-T

24093140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135502822-T-C

24093140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135502822-T-G

24093145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135502817-G-A

24093145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135502817-G-T

24093149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135502813-T-A

24093149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135502813-T-C

24093149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135502813-T-G

24093332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135502619-G-A

24093712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135502119-G-A

24093717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135502114-C-G

24093717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135502114-C-T

http://identifiers.org/hco/1/GRCh38#24093764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135502067-C-A

24093829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135502008-G-A

24093829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135502008-G-C

http://identifiers.org/hco/1/GRCh38#24094978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135501602-C-A

24095346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135501188-G-A

24095346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135501188-G-T

24095374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135501164-A-G

24095374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 135501164-A-T

24095416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135501146-G-T

http://identifiers.org/hco/1/GRCh38#24095426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135501134-C-A

24095426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135501134-C-G

24095426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135501134-C-T

24095801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135500752-T-C

24095960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135500657-T-C

24096121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135500566-C-T

24096716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135500057-G-A

24096781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135499852-G-A

http://identifiers.org/hco/1/GRCh38#24096863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135499790-A-C

24096863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135499790-A-G

24096949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135499727-C-G

http://identifiers.org/hco/1/GRCh38#24096975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135499701-C-A

24096975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135499701-C-T

24096999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135499674-A-G

24097115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135499558-G-A

24097125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135499550-C-T

24097165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135499509-G-C

24097239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135499465-C-G

24097239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135499465-C-T

24097375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135499363-G-A

24097866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135498981-C-G

24097866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135498981-C-T

24097913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135498939-G-A

24097913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135498939-G-T

http://identifiers.org/hco/1/GRCh38#24097925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135498927-C-A

24097925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 135498927-C-T

24097963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135498889-G-A

24098075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498786-C-T

24098097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498773-G-T

http://identifiers.org/hco/1/GRCh38#24098100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135498770-C-A

24098170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498701-T-G

24098482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498379-T-A

24098482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498379-T-G

http://identifiers.org/hco/1/GRCh38#24099552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135498185-C-A

24099552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498185-C-T

24099577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498160-G-A

24099584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498152-T-A

24099584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498152-T-C

24099586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498150-G-C

24099586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498150-G-T

24099639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498115-A-T

24099644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498110-C-G

24099655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498099-G-A

24099655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498099-G-C

24099655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135498099-G-T

24099681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 135498074-T-C

24099764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 135497991-T-C

http://identifiers.org/hco/1/GRCh38#24099843-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135497935-A-C

24099843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135497935-A-T

24102044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135496435-C-T

24102064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135496408-C-T

24102115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135496349-G-C

http://identifiers.org/hco/1/GRCh38#24102222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135496248-C-A

24102222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135496248-C-G

24102327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135496161-G-T

http://identifiers.org/hco/1/GRCh38#24103130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135494614-C-A

http://identifiers.org/hco/1/GRCh38#24103270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135494535-A-C

24103270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135494535-A-G

24103290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135494515-C-T

24103417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135494388-T-C

24105087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135493749-C-T

24105160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135493670-G-T

24105213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135493565-T-C

24105301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135493476-G-A

24105373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135493406-G-A

24105698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135493113-C-T

24105801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135493092-G-A

24105801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135493092-G-T

24105836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135493057-A-G

24105889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135493043-C-G

24105898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135493034-C-T

24106022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135492908-C-T

24106036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135492894-C-T

24106073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 135492857-T-C

24106205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492768-T-A

24106205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492768-T-C

24106223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492748-T-C

24106953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492367-T-C

http://identifiers.org/hco/1/GRCh38#24106955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135492365-C-A

24106955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492365-C-T

24106957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492363-G-A

24106957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492363-G-T

http://identifiers.org/hco/1/GRCh38#24106961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135492359-C-A

24106962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492358-A-G

24107024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492304-G-A

24107024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492304-G-T

24107025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492303-G-A

24107025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492303-G-C

24107025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492303-G-T

http://identifiers.org/hco/1/GRCh38#24107044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135492284-C-A

24107044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492284-C-T

24107063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492267-A-G

24107063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135492267-A-T

24107169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135492161-C-T

24107208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135492122-G-A

24107208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 135492122-G-T

24107509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135491456-C-T

24107842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135491180-T-C

24107857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135491166-G-A

24107857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135491166-G-T

24107871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135491156-T-A

http://identifiers.org/hco/1/GRCh38#24107872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135491155-C-A

24107907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135491115-G-A

24107907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135491115-G-C

24107907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 135491115-G-T

24108085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135490940-A-G

http://identifiers.org/hco/1/GRCh38#24108108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135490918-C-A

24108108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135490918-C-T

24108129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135490899-T-A

24108129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135490899-T-C

http://identifiers.org/hco/1/GRCh38#24108140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135490888-C-A

24108140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135490888-C-T

24108143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135490885-C-T

24108232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135490796-C-G

24108303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135490134-G-A

24108303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135490134-G-T

http://identifiers.org/hco/1/GRCh38#24108350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135490118-C-A

24108350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135490118-C-G

24108411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 135490058-T-C

24108467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, undefined
orthologous variants: 135490006-G-T

http://identifiers.org/hco/1/GRCh38#24108579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/4/GRCm39#135489886-C-A

24108579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense variant
orthologous variants: 135489886-C-T

24108582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense variant
orthologous variants: 135489883-T-A

24108582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense variant
orthologous variants: 135489883-T-C

http://identifiers.org/hco/1/GRCh38#24108611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135489854-C-A

24108611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: missense variant
orthologous variants: 135489854-C-T

24108662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 135489803-G-A

24108662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 135489803-G-T

http://identifiers.org/hco/1/GRCh38#24108664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135489801-C-A

24108664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, undefined
orthologous variants: 135489801-C-T

http://identifiers.org/hco/1/GRCh38#24108672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#135489793-C-A

24108672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, undefined
orthologous variants: 135489793-C-T

24108698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, undefined
orthologous variants: 135489763-T-C

24108705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135489756-T-C

http://identifiers.org/hco/1/GRCh38#24108720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135489692-C-A

http://identifiers.org/hco/1/GRCh38#24108723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135489689-A-C

24108733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135489681-G-A

http://identifiers.org/hco/1/GRCh38#24108777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135489517-C-A

24108777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135489517-C-T

24108804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135489490-G-T

24108824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135489475-G-T

24108869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron_variant, undefined
orthologous variants: 135489443-C-T

http://identifiers.org/hco/1/GRCh38#24108992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135489353-C-A

24109080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135489267-T-G

24109152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135489214-C-T

24109378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135489010-G-A

24109384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135489006-T-A

24109384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135489006-T-C

24109470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135488923-T-A

24109471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135488922-C-T

24110636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135488723-A-G

24111242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135488300-G-A

24111377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135488284-T-A

24111470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135488221-T-C

24111632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135488062-G-A

24111659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135488027-G-A

24111841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135487845-C-G

24111886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135487799-G-C

24111886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135487799-G-T

http://identifiers.org/hco/1/GRCh38#24111895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135487790-C-A

24111895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135487790-C-T

24111934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135487749-G-A

24111934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135487749-G-T

http://identifiers.org/hco/1/GRCh38#24111937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135487746-C-A

24111937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135487746-C-T

24111951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135487199-T-C

http://identifiers.org/hco/1/GRCh38#24111973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135487166-C-A

24111973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135487166-C-G

24111973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: intron variant
orthologous variants: 135487166-C-T

http://identifiers.org/hco/1/GRCh38#24112030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: splice donor variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135487116-C-A

24112030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: splice donor variant
orthologous variants: 135487116-C-T

24112038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 5 prime UTR variant
orthologous variants: 135487108-G-A

http://identifiers.org/hco/1/GRCh38#24112047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#135487098-C-A

24112047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 5 prime UTR variant
orthologous variants: 135487098-C-T

24112051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 5 prime UTR variant
orthologous variants: 135487094-G-A

24112057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 5 prime UTR variant
orthologous variants: 135487088-T-C

24112125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26679
most severe consequence: 5 prime UTR variant
orthologous variants: 135487034-G-A