42273217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234351-C-T

42273306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 120234437-C-G

42273306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 120234437-C-T

42273443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 120234598-C-T

42273536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234663-G-A

42273536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234663-G-T

42273545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234672-T-A

42273553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120234680-T-A

42273553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120234680-T-C

http://identifiers.org/hco/15/GRCh38#42273609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120234745-C-A

42273609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120234745-C-T

http://identifiers.org/hco/15/GRCh38#42273657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120234783-C-A

42273657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120234783-C-T

42273687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234813-A-G

42273708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234824-G-A

42273708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234824-G-C

42273708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234824-G-T

42273731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234843-G-A

42273731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234843-G-T

42273745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234857-T-A

42273745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234857-T-C

42273765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120234877-G-T

http://identifiers.org/hco/15/GRCh38#42273814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#120234923-C-A

42273814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234923-C-G

42273814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234923-C-T

http://identifiers.org/hco/15/GRCh38#42273840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#120234949-C-A

42273840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120234949-C-T

http://identifiers.org/hco/15/GRCh38#42273933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120235025-C-A

42273933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120235025-C-T

http://identifiers.org/hco/15/GRCh38#42273934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120235026-C-A

42273934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120235026-C-T

http://identifiers.org/hco/15/GRCh38#42273942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120235034-C-A

42273942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120235034-C-T

http://identifiers.org/hco/15/GRCh38#42273958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120235053-C-A

42273958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120235053-C-T

http://identifiers.org/hco/15/GRCh38#42274015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#120235111-C-A

42274015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120235111-C-T

http://identifiers.org/hco/15/GRCh38#42274189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#120235251-C-A

42274189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120235251-C-T

http://identifiers.org/hco/15/GRCh38#42274293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120235336-C-A

42274293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120235336-C-T

42274415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120235443-T-A

42274475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 120235505-A-G

42274488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120235518-G-C

42274488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120235518-G-T

http://identifiers.org/hco/15/GRCh38#42274542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120235560-C-A

42274610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120235652-G-C

42274610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120235652-G-T

42275800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120236281-C-T

42276105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120236510-C-T

42276208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120236620-G-C

42276211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120236623-G-T

42276296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120236694-G-A

42276296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120236694-G-C

42276296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120236694-G-T

42276363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120236762-T-C

42276363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120236762-T-G

42276376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120236775-A-G

42276427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120236821-T-A

42276427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120236821-T-C

42276427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120236821-T-G

42276451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120236842-G-A

42276451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120236842-G-T

42276454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120236845-A-G

42276454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120236845-A-T

42276455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120236846-G-A

42276455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120236846-G-T

42277221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120237661-C-T

http://identifiers.org/hco/15/GRCh38#42278476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120241910-C-A

42278476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120241910-C-T

http://identifiers.org/hco/15/GRCh38#42278508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120241942-A-C

42278508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120241942-A-G

42278648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120242068-A-G

42278648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120242068-A-T

42279076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120242581-A-G

42279183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120242687-C-T

42279238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120242742-T-G

http://identifiers.org/hco/15/GRCh38#42279305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120242804-C-A

42279305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120242804-C-T

42279414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120242892-G-A

http://identifiers.org/hco/15/GRCh38#42279616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#120243182-C-A

42280693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120243931-C-G

42280776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120244024-A-G

http://identifiers.org/hco/15/GRCh38#42280809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120244056-C-A

42280889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120244142-T-A

42280889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120244142-T-C

42280953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120244321-G-A

http://identifiers.org/hco/15/GRCh38#42280973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120244341-C-A

42281094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120244442-G-C

42281127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 120244471-T-C

42282455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120244680-C-G

42282455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120244680-C-T

42282499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120244729-C-T

42282951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120245139-G-A

42282994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120245183-C-T

42283328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120245285-G-C

42283461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120245402-A-G

42283462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120245403-G-A

http://identifiers.org/hco/15/GRCh38#42286247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120248210-C-A

42286247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120248210-C-G

42286247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120248210-C-T

42286546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120248473-C-T

42286555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120248482-A-G

42286771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120248635-C-T

42286963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120248829-G-A

42287071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120248926-G-A

42287071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120248926-G-T

42287143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120249003-C-T

42287147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120249007-G-A

42287419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120249570-T-C

42287419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120249570-T-G

42287452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120249604-G-T

42287461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120249613-A-G

42287569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120249715-G-T

42287638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 120249785-T-C

42287711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120249859-T-G

42287758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120249906-C-T

42287897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120250061-G-A

42287897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120250061-G-T

http://identifiers.org/hco/15/GRCh38#42288212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120250338-C-A

42288212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120250338-C-T

42288489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120250597-T-G

42292562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120252350-A-G

42292778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120252546-G-C

42292778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120252546-G-T

http://identifiers.org/hco/15/GRCh38#42292828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120252596-A-C

42292835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120252603-G-A

42292956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120252726-A-G

42297551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254119-T-C

http://identifiers.org/hco/15/GRCh38#42297576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120254144-C-A

42297576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254144-C-T

42297577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254145-A-G

42297748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254314-G-C

42297754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254320-T-C

42297771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254337-G-A

42297771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254337-G-T

42297776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254342-T-A

42297776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254342-T-C

42297776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254342-T-G

42297793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254362-T-C

42297808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254377-T-A

42297808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254377-T-C

42297808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254377-T-G

42298254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254538-G-A

42298254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254538-G-T

42298286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254574-A-G

42298328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254615-G-A

42298328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254615-G-T

42298458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254746-A-G

42298598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120254877-G-A

42306520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258185-G-A

42306667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258371-A-G

42306748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258562-G-C

42306748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120258562-G-T

42308139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120259203-A-G

42308332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120259392-A-G

42308346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120259406-A-G

42308580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120259779-T-A

42308580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120259779-T-C

42308693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120259920-G-T

42308704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120259931-C-T

42309304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120260586-G-A

42310199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120260976-T-G

42310471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120261224-A-G

http://identifiers.org/hco/15/GRCh38#42310477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120261230-C-A

42310481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120261234-G-A

42310493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120261246-A-G

42310537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120261273-A-G

42310574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120261309-A-G

42310574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120261309-A-T

42310638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120261369-G-A

42310638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120261369-G-T

42310699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120261428-C-G

42310699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120261428-C-T

42321590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120263945-A-G

42321801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120264119-C-G

42321801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120264119-C-T

42321912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120264230-G-A

http://identifiers.org/hco/15/GRCh38#42321948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#120264266-C-A

42322054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120264372-T-A

42326100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265593-A-G

42326246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265698-C-T

42326348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120265794-A-G

42326348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120265794-A-T

http://identifiers.org/hco/15/GRCh38#42326492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120265926-C-A

42326493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265927-A-G

42326563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120265992-A-T

http://identifiers.org/hco/15/GRCh38#42327244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120266979-C-A

42327244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120266979-C-T

http://identifiers.org/hco/15/GRCh38#42327279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120267019-C-A

42327279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120267019-C-G

42327288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120267028-G-C

42327288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120267028-G-T

http://identifiers.org/hco/15/GRCh38#42327301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120267041-C-A

42327301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120267041-C-G

42327301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120267041-C-T

42327304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120267044-T-C

http://identifiers.org/hco/15/GRCh38#42327339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120267079-C-A

42327339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120267079-C-T

42328489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120269049-G-A

42328489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120269049-G-T

http://identifiers.org/hco/15/GRCh38#42328526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120269094-C-A

42328526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120269094-C-G

42328564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120269136-G-A

42329263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120269736-C-T

42329285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120269760-T-C

42329292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120269767-G-A

42329314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120269789-G-A

42329527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120269994-T-A

42329583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120270034-G-A

http://identifiers.org/hco/15/GRCh38#42329624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120270065-C-A

42329624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120270065-C-G

42329624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120270065-C-T

http://identifiers.org/hco/15/GRCh38#42329643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120270085-C-A

http://identifiers.org/hco/15/GRCh38#42329768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120270148-A-C

http://identifiers.org/hco/15/GRCh38#42330221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120271541-C-A

42330221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120271541-C-T

42330484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120271884-T-C

42330502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120271902-T-C

42330523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120271922-T-G

42330573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120271982-T-C

42330573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120271982-T-G

42330605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: synonymous variant
orthologous variants: 120272014-A-G

42330656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: synonymous variant
orthologous variants: 120272065-T-G

42330734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120272149-A-T

42330746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120272161-T-A

http://identifiers.org/hco/15/GRCh38#42331461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120273073-A-C

42331561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120273176-C-T

42331686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120273279-G-T

42331722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120273309-C-T

42338286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120274515-T-A

http://identifiers.org/hco/15/GRCh38#42338327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120274557-C-A

42338345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120274573-T-A

42338345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120274573-T-C

42338345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120274573-T-G

42338381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120274612-G-T

42338459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: synonymous variant
orthologous variants: 120274689-T-C

42338471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: synonymous variant
orthologous variants: 120274701-T-C

42338471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: synonymous variant
orthologous variants: 120274701-T-G

http://identifiers.org/hco/15/GRCh38#42338502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120274732-C-A

42338502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120274732-C-T

42338513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120274746-T-C

42338523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120274756-G-A

42338526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120274759-A-G

42338551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120274779-A-G

42338551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120274779-A-T

42338934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120276100-C-T

42338992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120276151-A-G

42339166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120276340-C-T

42339268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120276421-G-A

42339282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120276435-T-G

42339371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120276483-G-C

42339551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120276664-T-C

42339552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120276665-G-A

42339552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120276665-G-T

42339631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120276740-A-G

42339679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: synonymous variant
orthologous variants: 120276790-C-T

42339884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: missense variant
orthologous variants: 120276995-G-A

http://identifiers.org/hco/15/GRCh38#42339933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120277042-C-A

42339959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120277065-T-C

42339964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120277070-G-A

http://identifiers.org/hco/15/GRCh38#42339970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120277076-A-C

42339970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120277076-A-G

42339976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120277082-T-C

http://identifiers.org/hco/15/GRCh38#42340024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120277108-C-A

42340024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120277108-C-G

42340024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120277108-C-T

http://identifiers.org/hco/15/GRCh38#42340629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120278802-A-C

42340629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120278802-A-G

42340629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120278802-A-T

42340630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120278803-G-A

42340630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120278803-G-T

42341075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120278947-G-T

42341182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120279042-T-C

42341261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120279498-A-T

42341281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120279534-T-G

42341437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120279972-G-A

42341480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120280013-A-G

42341504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120280037-A-G

42342011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120280356-T-C

42342116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120280447-G-C

42342441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120280651-G-A

42342823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120281068-T-G

42342953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120281183-T-C

42342953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120281183-T-G

42342958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120281188-C-T

42342962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120281192-A-G

42342965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120281195-G-T

42342977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120281207-G-A

42342977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120281207-G-T

42343026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120281250-T-G

42343119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: missense variant
orthologous variants: 120281343-A-G

42343123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: missense variant
orthologous variants: 120281347-C-T

42343130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: synonymous variant
orthologous variants: 120281354-T-C

http://identifiers.org/hco/15/GRCh38#42343174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120281399-C-A

42343174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120281399-C-T

42343293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron variant
orthologous variants: 120281561-T-C

42345799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120283115-G-A

42345922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120283221-T-C

42345984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120283261-A-G

42346696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120284104-A-G

42347138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120284828-G-A

42347192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120284882-G-A

42347196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120284886-A-G

42347200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120284890-A-G

42347430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120285148-G-A

42348009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120286392-G-T

42348026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120286409-A-G

42348052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120286424-G-A

42348052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120286424-G-T

42348063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120286435-A-G

42348063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120286435-A-T

42348105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 120286476-T-C

42348211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 120286582-A-G

42348449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 120286814-G-C

42348865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120287172-T-C

42349021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120287336-G-C

42349050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120287366-C-T

42349221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120287513-G-A

42349287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120287596-A-G

42349287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120287596-A-T

http://identifiers.org/hco/15/GRCh38#42349374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120287680-A-C

42349374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120287680-A-G

42349374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120287680-A-T

42349443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120287749-A-G

42349531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120287831-G-A

42349604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120288114-G-T

42349650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120288175-T-C

42351220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120288423-G-A

42351220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120288423-G-T

http://identifiers.org/hco/15/GRCh38#42351222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120288425-C-A

42351461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120288656-C-G

http://identifiers.org/hco/15/GRCh38#42351489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120288685-C-A

42351489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120288685-C-T

42351493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120288692-G-T

42351812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120290072-A-G

42351855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120290115-T-C

http://identifiers.org/hco/15/GRCh38#42351881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120290141-C-A

42351881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120290141-C-T

42351901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120290160-A-G

42351902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120290161-G-A

42351923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120290186-G-A

42351923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120290186-G-T

42351975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120290243-T-C

42351975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120290243-T-G

42351985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120290253-T-C

42352077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120290344-A-G

42352077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120290344-A-T

42352107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120290374-A-G

http://identifiers.org/hco/15/GRCh38#42352151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120290417-C-A

42352178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120290442-T-C

42352237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120290496-T-C

http://identifiers.org/hco/15/GRCh38#42352246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120290504-C-A

http://identifiers.org/hco/15/GRCh38#42352386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120290761-A-C

42352458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120290785-G-A

42352458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120290785-G-T

42352462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120290789-G-A

42352462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120290789-G-T

42352505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120290830-G-A

42352505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120290830-G-T

42352596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120290921-T-A

42352596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120290921-T-C

42352622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120290948-G-A

http://identifiers.org/hco/15/GRCh38#42352675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120291001-C-A

42352675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291001-C-G

42352675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291001-C-T

42352719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291043-T-A

http://identifiers.org/hco/15/GRCh38#42352791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120291118-C-A

42352791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291118-C-T

42352846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291178-G-A

42352846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291178-G-C

42352899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291230-G-A

42352899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291230-G-C

42352899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291230-G-T

42352995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291304-A-T

http://identifiers.org/hco/15/GRCh38#42353100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120291416-A-C

42353100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291416-A-G

http://identifiers.org/hco/15/GRCh38#42353127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120291443-A-C

42353127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291443-A-G

42353165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291448-G-C

42353165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291448-G-T

42353184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291467-G-A

42353184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291467-G-T

42353219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291501-G-C

http://identifiers.org/hco/15/GRCh38#42353226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120291508-C-A

42353226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291508-C-T

42353227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291509-T-C

42353260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291531-T-C

42353374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291655-T-C

42353374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291655-T-G

http://identifiers.org/hco/15/GRCh38#42353384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120291665-C-A

42353384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291665-C-T

42353391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291672-G-T

http://identifiers.org/hco/15/GRCh38#42353433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120291716-C-A

42353433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291716-C-T

http://identifiers.org/hco/15/GRCh38#42353473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120291756-C-A

42353473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291756-C-T

42353514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291796-T-A

42353523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4139
most severe consequence: 3 prime UTR variant
orthologous variants: 120291807-T-C