149517393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57363241-G-A

149517396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57363244-G-A

http://identifiers.org/hco/3/GRCh38#149517561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57363408-C-A

149517569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57363416-C-T

149517583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57363426-A-T

149517595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57363438-G-A

149517599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57363443-G-T

149517748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57363579-G-A

149517816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57363644-G-A

149517890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57363706-A-G

149518408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57364274-C-T

http://identifiers.org/hco/3/GRCh38#149518692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57364556-C-A

149518698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57364564-C-T

149518743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57364615-G-A

149518821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57364676-T-A

149518858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57364713-G-T

149518860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57364715-G-A

http://identifiers.org/hco/3/GRCh38#149518877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57364732-C-A

149518877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57364732-C-T

149518882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57364736-C-T

149519278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57365146-T-C

149519313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57365181-A-G

http://identifiers.org/hco/3/GRCh38#149519568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57365433-C-A

149519956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57365594-A-G

http://identifiers.org/hco/3/GRCh38#149519960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57365598-C-A

149520085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57365669-G-A

149520085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57365669-G-T

http://identifiers.org/hco/3/GRCh38#149520164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57365737-C-A

149520164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57365737-C-T

149520273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57365845-C-T

149520275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3 prime UTR variant
orthologous variants: 57365847-G-T

149520715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 57366256-G-A

149520715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 57366256-G-T

http://identifiers.org/hco/3/GRCh38#149520763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57366304-A-C

149520767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 57366310-G-A

149521013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57366555-A-G

149524109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57368208-G-C

http://identifiers.org/hco/3/GRCh38#149524194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57368286-C-A

149524522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57368514-A-T

149524562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57368556-C-T

http://identifiers.org/hco/3/GRCh38#149524595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57368581-C-A

149524650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57368636-A-G

149524931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57369118-G-A

149524961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57369148-T-C

149525071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57369352-C-T

149525078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57369399-C-G

149525091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57369424-G-A

149525362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 57369682-A-G

149526005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 57369932-G-T

http://identifiers.org/hco/3/GRCh38#149526122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57370049-C-A

149526122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57370049-C-T

149526309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57370226-G-A

149526446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57370353-T-C

149527505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57370599-T-C

149527561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57370652-C-T

149527597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57370687-T-C

149527724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57370756-A-G

149527792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57370821-T-A

149527984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57371005-G-A

http://identifiers.org/hco/3/GRCh38#149528033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57371050-C-A

http://identifiers.org/hco/3/GRCh38#149528121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57371131-C-A

149528264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57371271-T-A

149528994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57371899-G-A

149529010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57371904-G-C

http://identifiers.org/hco/3/GRCh38#149529111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57371990-A-C

149531242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57373982-T-C

149531921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57374602-T-C

149531924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57374605-G-A

149532252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57374957-T-C

http://identifiers.org/hco/3/GRCh38#149532547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57375292-C-A

149532547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57375292-C-T

149533260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57376691-C-T

149533543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57376915-C-G

http://identifiers.org/hco/3/GRCh38#149533685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57377055-A-C

149533685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57377055-A-G

149534510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57378087-T-C

149534953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57378493-T-C

149535043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57378580-C-T

149535053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57378601-G-A

http://identifiers.org/hco/3/GRCh38#149535166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57378714-A-C

149535233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57378780-T-A

149535319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57378867-T-C

149535344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57378894-G-A

149535364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57378900-G-A

149535370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57378906-C-T

149535371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57378907-G-A

149536303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57379729-C-T

149536315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57379741-A-G

149536368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57379791-C-T

149536412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57379830-T-A

149536415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57379833-T-C

149536562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57379951-T-C

149536564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57379953-G-A

149536575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57379964-T-C

149536630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57380025-G-A

149536740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57380141-C-T

149538572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57380951-G-A

149538591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57380968-T-C

http://identifiers.org/hco/3/GRCh38#149538763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57381106-A-C

149539014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57381349-C-G

149539036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57381371-T-G

149539083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57381418-A-G

149539115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57381452-T-C

149539502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57381598-C-T

149539508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57381604-C-T

149539672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57381750-A-T

149539719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57381798-A-G

149539907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57382347-T-C

149539947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57382391-C-T

149540062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57382515-T-C

149540087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57382541-C-T

149540133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57382585-G-A

149540133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57382585-G-T

149540256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57382680-G-A

149540256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57382680-G-T

149540444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57382859-C-T

149540930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57383255-T-C

149541474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57384010-G-A

149542512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: synonymous_variant, undefined
orthologous variants: 57384952-C-T

149542555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57384995-A-G

149542586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57385026-T-A

149544082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57386410-C-G

149545100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57386628-T-C

149545460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57386945-T-C

149545805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57387148-G-A

149545805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57387148-G-T

149545877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57387203-A-G

149545927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57387254-G-C

149545964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57387289-G-A

149546282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57387634-C-T

149546374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57387827-T-C

149546519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57388092-C-T

149546553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57388122-G-A

149546825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57388634-G-A

149546864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57388665-C-T

149546912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57388697-T-C

149546970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57388748-A-G

149547013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57388792-A-G

149547104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57388870-G-A

149547187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57388934-T-C

149547203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57388950-A-G

149547220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57388967-T-A

149547586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57388990-T-A

149547626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57389029-G-C

149547656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57389059-C-T

149547856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57389208-C-T

149548068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57389350-G-A

149548069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57389351-G-T

149548075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57389357-T-C

149548176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57389497-C-T

149548177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57389498-G-A

149548280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57389567-A-G

149548336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57389627-G-A

149548343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57389637-A-T

149548556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57389848-A-G

149548594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57389882-T-A

149548614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57389902-G-A

http://identifiers.org/hco/3/GRCh38#149548618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#57389906-A-C

149548622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57389910-G-C

149548935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57390186-T-A

149548946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57390196-T-C

149548946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57390196-T-G

149548947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57390197-A-G

149549203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57390415-T-C

149549410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57390660-T-C

149549447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57390697-C-T

149550618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57392906-C-T

149550754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57393083-T-C

149550779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57393107-T-A

149550781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57393111-A-T

149550798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57393128-G-A

149551154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57393357-G-A

149551247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57393441-A-G

http://identifiers.org/hco/3/GRCh38#149551296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57393476-C-A

149551334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57393508-T-C

149551392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57393565-G-A

149551402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57393574-G-A

149551538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57393708-G-A

http://identifiers.org/hco/3/GRCh38#149551679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57393825-C-A

149551679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57393825-C-G

149552800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57394123-T-A

149553029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57394334-A-G

149553053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57394356-C-G

149553511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57394722-C-T

http://identifiers.org/hco/3/GRCh38#149553619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57394813-C-A

149553816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57394987-A-G

149553844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57395011-G-A

149553950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57395099-G-A

149554104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57395264-T-C

149554154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57395314-C-T

149554315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57395428-G-A

149554368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57395469-A-G

149554549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57395650-A-G

http://identifiers.org/hco/3/GRCh38#149554697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57395810-C-A

149554836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57395988-G-A

149555453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57396347-A-T

http://identifiers.org/hco/3/GRCh38#149555477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57396368-C-A

149555477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57396368-C-T

149555492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57396383-A-G

149555684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57396562-G-A

149555687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57396565-G-T

149555707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57396586-T-C

149555712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57396591-G-C

149555717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57396600-T-C

149555790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57396636-T-C

149555820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57396666-G-A

149556010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57397179-C-T

149556024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57397199-T-C

149556092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57397265-G-A

http://identifiers.org/hco/3/GRCh38#149556097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57397270-C-A

149556124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57397297-G-T

149556203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57397375-C-G

149556634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57397420-G-A

149556723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57397518-C-G

149556757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57397550-C-T

149558372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57398964-G-C

149558505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57399093-G-A

149558520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57399106-A-G

149558586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57399158-T-C

149558626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57399187-A-T

149558905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57399673-G-A

149558905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57399673-G-C

149558958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57399729-A-G

149559134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57399920-A-T

149559745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57400414-A-T

149559774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57400446-A-G

149559830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57400552-C-T

149559891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57400590-A-T

149560126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57400808-T-C

149560188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57400875-A-G

149560209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57400896-G-A

149560406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57401120-T-C

149560439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57401152-T-C

http://identifiers.org/hco/3/GRCh38#149560644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57401354-A-C

149560747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57401458-C-T

149561004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57402088-T-A

149561111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57402202-G-A

149561498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57402813-T-C

149561565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57402876-T-C

149561693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57402967-G-A

149561877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57403119-G-T

149561959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57403183-G-C

149562346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57403500-A-G

149562347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57403501-C-T

149562651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57403913-G-A

149562651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57403913-G-C

http://identifiers.org/hco/3/GRCh38#149562898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57404184-C-A

149562942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57404216-A-G

149563058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57404360-A-T

149568357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57404715-G-A

http://identifiers.org/hco/3/GRCh38#149568552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57404886-A-C

149568552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57404886-A-G

149568691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57405031-T-G

149570842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57406116-C-T

149570930-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57406248-T-A

149570979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57406297-T-C

149570992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57406310-T-C

149571062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57406375-G-C

149571159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57406489-C-T

149571418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57407650-C-T

149571600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57407794-C-T

149571633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57407809-G-A

149571645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57407821-G-A

149571683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57407858-G-T

149571796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57407974-T-C

149572642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57408775-C-T

149572852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57409141-C-T

149572987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: missense variant
orthologous variants: 57409276-T-C

149573046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57409335-A-G

149573134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57409425-G-T

http://identifiers.org/hco/3/GRCh38#149573917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57409703-A-C

149574450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57409923-G-A

149574749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57410406-G-A

http://identifiers.org/hco/3/GRCh38#149575098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57410668-A-C

149575098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57410668-A-G

149575524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57411470-A-G

149575742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57411681-G-A

http://identifiers.org/hco/3/GRCh38#149575834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57411742-A-C

http://identifiers.org/hco/3/GRCh38#149575895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57411811-C-A

149576048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57412020-G-A

149576048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57412020-G-T

149576136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57412122-G-A

http://identifiers.org/hco/3/GRCh38#149576141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57412127-C-A

149576141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57412127-C-G

http://identifiers.org/hco/3/GRCh38#149576209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57412199-C-A

http://identifiers.org/hco/3/GRCh38#149576302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57412289-C-A

149576309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57412296-C-T

149576317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57412304-T-C

149576610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57412576-A-G

149577185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57413262-A-G

149577185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57413262-A-T

http://identifiers.org/hco/3/GRCh38#149577206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57413277-C-A

149577634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57413660-A-G

149577861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57413854-G-A

149577861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57413854-G-C

http://identifiers.org/hco/3/GRCh38#149578278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57414245-C-A

149578370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57414346-A-G

149578520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57414481-T-G

149578522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57414483-C-T

149579835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57415548-A-G

149581403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57416833-T-C

149581441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57416861-A-G

149583740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57418739-A-T

149583783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57418779-C-G

149584326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57419673-G-A

149584326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57419673-G-C

149584512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57419860-A-G

149584577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57419923-C-T

http://identifiers.org/hco/3/GRCh38#149584773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57420141-A-C

149584773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57420141-A-G

http://identifiers.org/hco/3/GRCh38#149588477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57421983-C-A

149588477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57421983-C-G

149588585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57422112-G-A

149588663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57422177-C-T

149588896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57422847-A-T

149588995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57422941-G-A

149589035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57422977-C-T

149589522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57423698-C-T

149589770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57424023-T-C

http://identifiers.org/hco/3/GRCh38#149590096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57424515-C-A

149590100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57424519-A-G

149590181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57424610-G-A

149590283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57424678-A-G

149590690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57424779-T-G

149590725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57424814-T-A

149590757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57424832-T-G

149590773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57424848-T-C

149590841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57424913-G-A

149590877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57424949-C-G

149590949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57425017-T-C

149590968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57425035-C-T

149592211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57426668-A-G

149592418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57426978-T-C

149592420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57426980-C-T

149592459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57427019-T-A

149592838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57427588-C-T

149592950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57427698-C-T

149593029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57427772-T-C

149593180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57427918-T-C

149593278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57427993-G-T

149593283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57428000-C-T

149593331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57428063-C-T

http://identifiers.org/hco/3/GRCh38#149593411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57428130-C-A

149596205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57429420-G-T

149596506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57429616-C-T

149596539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57429692-T-C

149596556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57429724-C-T

149596584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57429754-G-C

149596679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57429879-T-C

149596730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57429937-A-G

http://identifiers.org/hco/3/GRCh38#149596755-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57429970-A-C

149597131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57430355-G-A

http://identifiers.org/hco/3/GRCh38#149597221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57430440-C-A

149597265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57430483-C-T

http://identifiers.org/hco/3/GRCh38#149598853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57433574-C-A

149600220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57438926-T-C

149600337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57439029-A-G

http://identifiers.org/hco/3/GRCh38#149600397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57439083-C-A

149600397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57439083-C-T

149600472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57439156-A-G

149600808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57439732-T-C

149601055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57439947-T-C

149601058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57439950-C-G

149601109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57440000-G-A

149601164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57440055-G-A

149601164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57440055-G-C

149601625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57441028-A-G

149602273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57441318-A-G

149602482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57441513-G-A

149602482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57441513-G-T

149602509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57441525-T-A

149602509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57441525-T-C

http://identifiers.org/hco/3/GRCh38#149602764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57441658-A-C

http://identifiers.org/hco/3/GRCh38#149603554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57442373-C-A

149603554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57442373-C-G

149603554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57442373-C-T

149604206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57442971-G-C

149604246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57443000-C-T

149604355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57443129-C-G

149604355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57443129-C-T

149604630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57443398-A-G

149605124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57443803-T-C

149605130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57443809-G-A

149605130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57443809-G-C

149605432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57444097-G-C

149605517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57444177-C-T

149605734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57444305-A-G

149605735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57444306-G-A

http://identifiers.org/hco/3/GRCh38#149606574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57445285-A-C

149606651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57445352-G-C

149606917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57445658-C-T

149607258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57446973-T-C

149607258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57446973-T-G

149607863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57447416-G-A

149609233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57448329-G-A

149609565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57448565-A-T

149609726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57448701-T-C

149610000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57448963-T-C

149610012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57448975-A-G

149610120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57449090-T-C

http://identifiers.org/hco/3/GRCh38#149610232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57449159-C-A

149610232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57449159-C-T

http://identifiers.org/hco/3/GRCh38#149610238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57449164-A-C

149610564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57449459-G-A

149610656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57449523-G-C

149610751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57449631-T-C

149610802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57449682-T-A

149610991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57449831-A-T

http://identifiers.org/hco/3/GRCh38#149611457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57450225-C-A

149611698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57450407-G-A

http://identifiers.org/hco/3/GRCh38#149611746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57450452-A-C

149611746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57450452-A-G

149611759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57450463-T-C

149611940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57450595-G-C

149611973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57450628-T-C

149612019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57450670-T-C

149612320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57450956-T-C

149612441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57451078-G-A

149615648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57451400-G-A

149615760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57451491-G-A

149615769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57451500-C-T

149615879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57451613-A-G

149616149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57451905-G-A

149616149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57451905-G-C

149616209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57451966-G-C

149616237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57451987-C-T

149616268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57452009-G-A

149616416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57452143-A-G

149616439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57452155-T-C

149617001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57452604-A-T

149617008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57452611-G-A

149617032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57452635-G-T

149617670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57453067-C-T

149617733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57453121-G-T

149617941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57453359-C-T

149618048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57453481-A-G

149618185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57453565-C-T

149618268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57453619-C-T

149618346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57453677-G-A

149618623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57453898-G-A

149618628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57453905-G-A

149619220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57454408-G-A

149619281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57454481-C-T

149619666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57454538-T-C

149619760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57454613-G-A

149620190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57455048-C-T

149620329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57455163-G-A

149620682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57455550-G-T

149620902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57455884-T-C

149620971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57455955-A-G

149620990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57455974-T-C

149621102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57456086-A-T

149621204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57456183-C-T

149621230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57456209-T-C

149621537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57456515-T-C

149621621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57456584-C-G

149621716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57456679-A-G

149621804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57456773-C-T

149621834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57456802-T-C

149621847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57456815-T-C

149621848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57456816-G-A

149621949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57456892-C-T

149621982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57456925-C-T

149622008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57456951-A-G

149622100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57457036-A-G

149622173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57457081-T-C

http://identifiers.org/hco/3/GRCh38#149622358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57457230-A-C

149622454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57457332-G-A

149622466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57457344-G-A

http://identifiers.org/hco/3/GRCh38#149623676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57458014-A-C

149623874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57458186-C-T

149624185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57458491-T-C

149625077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57459414-T-C

149625089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57459441-A-T

149625820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57459494-A-G

http://identifiers.org/hco/3/GRCh38#149626162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57459882-A-C

149626475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57460355-G-A

149626549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57460427-G-T

149627054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57461019-G-A

149627273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57461401-C-G

149627529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57461620-C-T

149627754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57461873-G-A

149628493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57461948-T-C

149628502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57461957-T-C

149629327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57462548-G-A

149630239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57462805-A-T

149630381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57462920-G-A

149630595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57463111-C-T

149630678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57463207-G-A

149631071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57463495-G-A

149631099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57463523-A-G

149631275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57463702-T-C

149632092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57464656-T-C

149632147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57464705-A-T

149632173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57464725-A-G

149632269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57464877-C-T

149632386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57464979-G-C

149632386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57464979-G-T

149632704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57465299-C-T

149633127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57465716-G-A

149633195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57465798-C-G

149633195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57465798-C-T

149633904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57466346-C-T

149634097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57466520-T-A

149634137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57466556-T-C

149634584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57467157-T-C

http://identifiers.org/hco/3/GRCh38#149636124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57467508-C-A

149636198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57467803-C-G

149637002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57468328-T-A

http://identifiers.org/hco/3/GRCh38#149637135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57468455-A-C

149637812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57468960-G-T

http://identifiers.org/hco/3/GRCh38#149640179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57471159-C-A

http://identifiers.org/hco/3/GRCh38#149640407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57471322-C-A

149641579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57474273-T-C

149641838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57474485-C-T

149642098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57474706-A-G

149643160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57475464-C-T

149643312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57475617-C-T

149643332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57475637-G-T

149643603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57476296-A-G

149652310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57478188-A-G

149652506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57478311-G-A

149652645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57478403-A-G

149652645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57478403-A-T

149652930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57478614-G-A

149653339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57479130-T-C

149653611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57479427-G-A

http://identifiers.org/hco/3/GRCh38#149653815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57479623-C-A

149655511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57480698-A-G

149655622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57480808-C-G

149655975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57481399-G-A

149655975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57481399-G-T

149655976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57481400-C-T

149656229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57481640-T-C

149656744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57482093-G-A

149656744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57482093-G-C

149656744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57482093-G-T

149656804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57482153-C-T

149656859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57482227-G-A

149656859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57482227-G-T

http://identifiers.org/hco/3/GRCh38#149657097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57482465-C-A

149657097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57482465-C-G

http://identifiers.org/hco/3/GRCh38#149657440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57482781-C-A

149657440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57482781-C-T

149657580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57482898-T-A

149657580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57482898-T-G

149657581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57482899-A-G

http://identifiers.org/hco/3/GRCh38#149657654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57482956-C-A

149657654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57482956-C-G

149657722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57482993-T-A

149657722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57482993-T-C

149657773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57483030-G-A

149658053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57483250-T-C

http://identifiers.org/hco/3/GRCh38#149658172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57483363-C-A

149658217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57483400-A-G

149658362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57483538-T-C

149658416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57483592-C-G

149658416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57483592-C-T

149658420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57483596-G-T

149658628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57483794-G-A

149658628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57483794-G-T

149659260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57484372-G-A

149660099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57486143-A-G

149660099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57486143-A-T

http://identifiers.org/hco/3/GRCh38#149660107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57486151-C-A

http://identifiers.org/hco/3/GRCh38#149660178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57486198-C-A

149660178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57486198-C-G

149660178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57486198-C-T

149660312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57486325-G-A

149660312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57486325-G-T

149660354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57486333-G-C

149660354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57486333-G-T

149660459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57486424-G-T

http://identifiers.org/hco/3/GRCh38#149660488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57486443-C-A

149662127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57490897-A-T

149662177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57490950-T-C

http://identifiers.org/hco/3/GRCh38#149662186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57490959-A-C

149662287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57491060-A-G

149662401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57491171-T-C

149662767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, undefined
orthologous variants: 57491504-G-A

149663748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57492055-G-A

http://identifiers.org/hco/3/GRCh38#149664037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57492309-C-A

149664226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57492488-G-C

http://identifiers.org/hco/3/GRCh38#149664228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57492490-C-A

149664499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57492727-C-T

149664500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57492728-G-A

149664500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57492728-G-C

149664501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57492729-T-C

149665887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57493265-T-C

149665897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57493279-T-G

149666037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57493494-G-A

149666087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57493543-A-G

149666253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57493695-T-C

149666325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57493773-G-T

http://identifiers.org/hco/3/GRCh38#149666450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57493972-A-C

149666500-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57494023-T-A

149668580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57496993-G-A

149668580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57496993-G-C

149668580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57496993-G-T

http://identifiers.org/hco/3/GRCh38#149668698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57497055-A-C

149669315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57497580-C-T

149669551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57498082-A-G

http://identifiers.org/hco/3/GRCh38#149669587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57498118-C-A

149669692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57498218-G-A

149669692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57498218-G-T

http://identifiers.org/hco/3/GRCh38#149670705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57502615-C-A

149670705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57502615-C-T

149670751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57502636-T-C

149670886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 57502924-A-G

149670935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57502975-T-C

149670967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57503007-C-T

149671164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57503195-A-G

149671331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57503352-G-C

149700650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57504879-G-A

149700792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57505016-G-A

149700835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57505058-C-T

149700912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron variant
orthologous variants: 57505136-C-T

149703029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57507575-T-C

http://identifiers.org/hco/3/GRCh38#149703039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57507585-C-A

149703039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57507585-C-T

http://identifiers.org/hco/3/GRCh38#149703043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57507589-C-A

149703043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57507589-C-G

149703087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57507630-A-G

149703110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57507653-A-G

http://identifiers.org/hco/3/GRCh38#149703149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57507692-C-A

149703196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57507739-G-T

149703224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57507767-A-G

149703285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 57507838-G-T

149703326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 57507879-C-T

149703465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57508017-C-G

149705575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57509804-T-C

149706676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57511675-T-C

149706885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57512005-A-G

149706914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57512034-A-G

149706987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57512100-C-G

149707710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57513069-T-C

149711053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57519753-G-A

149713191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57530766-C-T

149713234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57530801-T-C

149716849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57532617-T-C

149717289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57533003-G-C

149717317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57533030-G-T

149717375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57533066-T-A

149717455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57533144-T-G

149717729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57533367-G-A

149717729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 57533367-G-C

149717769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57533402-T-C

149717888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57533512-T-A

149717920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57533536-T-C

149730211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57539792-T-G

149730410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57539993-G-A

http://identifiers.org/hco/3/GRCh38#149734821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57543494-A-C

149734821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57543494-A-G

149735556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57543904-A-G

http://identifiers.org/hco/3/GRCh38#149736003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57544378-C-A

149736003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57544378-C-T

http://identifiers.org/hco/3/GRCh38#149736029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57544408-C-A

149736132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57544992-G-A

149736155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57545015-A-G

149736544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57545272-G-A

149736544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57545272-G-T

http://identifiers.org/hco/3/GRCh38#149736602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57545332-C-A

149736622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: non coding transcript exon variant
orthologous variants: 57545352-G-T

http://identifiers.org/hco/3/GRCh38#149736643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#57545371-C-A

149736694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24042
most severe consequence: non coding transcript exon variant
orthologous variants: 57545417-G-T