http://identifiers.org/hco/1/GRCh38#159055161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173296039-C-A

159055161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: non coding transcript exon variant
orthologous variants: 173296039-C-T

159055220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: non coding transcript exon variant
orthologous variants: 173295987-C-T

http://identifiers.org/hco/1/GRCh38#159055286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173295922-C-A

159055301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: non coding transcript exon variant
orthologous variants: 173295907-T-C

159062543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173292710-G-A

159062543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173292710-G-T

159062566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173292683-T-C

159062566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173292683-T-G

159062575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173292674-G-A

159062575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173292674-G-T

159062601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 173292648-A-G

159062649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173292603-T-C

159062654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173292598-C-G

159062654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173292598-C-T

159062674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173292578-T-C

159062686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 173292566-A-T

159062766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173292489-G-T

159062770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173292485-C-T

159062782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173292473-C-T

http://identifiers.org/hco/1/GRCh38#159062826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173292433-A-C

159062826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173292433-A-G

http://identifiers.org/hco/1/GRCh38#159062839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173292426-C-A

159062854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173292401-A-T

159062866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173292389-T-A

http://identifiers.org/hco/1/GRCh38#159062869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173292386-A-C

159062869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173292386-A-G

159063107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173292183-C-T

159063130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173292161-T-C

159063339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173291728-G-C

159063339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173291728-G-T

159063364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173291703-G-A

159063364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173291703-G-T

159063370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173291698-T-G

159063372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173291696-A-G

159063375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173291693-A-G

159063459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173291621-G-A

159063459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173291621-G-C

159063459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173291621-G-T

159063646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173291451-A-T

159063722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173291375-T-G

http://identifiers.org/hco/1/GRCh38#159063741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173291354-C-A

159064284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173291250-T-G

159064371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173291168-A-G

159064434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173291103-G-A

http://identifiers.org/hco/1/GRCh38#159064821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173291030-C-A

159065067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173290798-T-C

159065296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173290573-G-T

159065350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173290543-G-A

159065547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173290392-T-C

159065792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173290068-T-C

159065808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173290007-C-G

159065808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173290007-C-T

159065840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289963-G-C

159065840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289963-G-T

159065893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289901-T-C

159065932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173289862-T-C

159065983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173289811-T-G

159066035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173289765-C-T

http://identifiers.org/hco/1/GRCh38#159066049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173289751-C-A

159066049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173289751-C-T

159066168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173289632-T-G

159066175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173289625-T-C

http://identifiers.org/hco/1/GRCh38#159066254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173289546-C-A

159066254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173289546-C-G

159066310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173289490-A-G

159066347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289454-A-T

159066385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289422-G-T

159066430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289389-G-A

159066430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289389-G-T

159066437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289382-G-A

159066437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289382-G-T

159066461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289359-G-A

159066461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289359-G-C

159066461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289359-G-T

159066545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289295-A-G

159066565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289275-G-A

159066698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289166-G-A

159066774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173289103-A-G

159066961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173288802-G-A

http://identifiers.org/hco/1/GRCh38#159067023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173288714-C-A

http://identifiers.org/hco/1/GRCh38#159067383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173288386-A-C

159067723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173288076-G-T

159067767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173288032-G-A

159067830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173287980-T-C

159067830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173287980-T-G

159068046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173287857-G-A

159068455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173287504-C-G

159068455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173287504-C-T

http://identifiers.org/hco/1/GRCh38#159068498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173287457-C-A

http://identifiers.org/hco/1/GRCh38#159068609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173287372-C-A

159068609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173287372-C-G

159068609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 173287372-C-T

http://identifiers.org/hco/1/GRCh38#159070464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173285582-A-C

159070464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173285582-A-G

159070589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173285456-T-A

159070589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173285456-T-C

159070650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173285404-T-C

159070706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173285362-T-G

159071912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173284350-G-T

159072356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173283949-T-A

159072652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173283662-T-C

159073097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173283279-G-A

159073097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173283279-G-T

http://identifiers.org/hco/1/GRCh38#159073101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173283275-C-A

159073372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173283045-G-A

http://identifiers.org/hco/1/GRCh38#159073426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173282991-A-C

http://identifiers.org/hco/1/GRCh38#159073462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173282955-C-A

159073482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 173282935-C-T

159073538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173282880-A-G

159073538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173282880-A-T

http://identifiers.org/hco/1/GRCh38#159073549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173282869-C-A

159073549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173282869-C-T

159073587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173282832-G-C

http://identifiers.org/hco/1/GRCh38#159073592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173282827-C-A

159073616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173282809-T-C

159073633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173282793-T-A

159073633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173282793-T-C

159073651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173282775-G-C

159073651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173282775-G-T

http://identifiers.org/hco/1/GRCh38#159074950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173282186-C-A

159075095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173282051-C-T

159075382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173281780-A-T

http://identifiers.org/hco/1/GRCh38#159075432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173281730-A-C

159075520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173281663-G-A

159075733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173281536-T-G

159076042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173281238-A-G

159076114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173281161-G-C

159076153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173281119-A-G

159076253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173281023-C-T

159076505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173277578-A-G

http://identifiers.org/hco/1/GRCh38#159076510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173277574-C-A

159076551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173277534-G-A

http://identifiers.org/hco/1/GRCh38#159076552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173277533-C-A

159076552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173277533-C-T

http://identifiers.org/hco/1/GRCh38#159076581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173277507-A-C

159076581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173277507-A-G

159076624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173277475-G-A

159076624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173277475-G-T

159076837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173277337-A-G

159076866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173277309-G-T

http://identifiers.org/hco/1/GRCh38#159076879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173277301-C-A

159076879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173277301-C-T

http://identifiers.org/hco/1/GRCh38#159083397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173270891-A-C

159083444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173270688-G-C

http://identifiers.org/hco/1/GRCh38#159083486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173270644-A-C

159084222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173269751-T-C

159084392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173269297-G-A

http://identifiers.org/hco/1/GRCh38#159084458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173269231-A-C

159084963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173269108-A-T

159085014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173269057-C-T

159085061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173269010-A-G

159085156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173268909-G-T

159085637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173268337-G-A

159085718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173268267-C-T

159085735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173268258-T-C

http://identifiers.org/hco/1/GRCh38#159085759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173268237-A-C

159085802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173268194-C-T

159085926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173268014-C-G

http://identifiers.org/hco/1/GRCh38#159085928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173268012-A-C

159085930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173268010-G-A

159086191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173267713-C-G

159086379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173267542-A-T

159086817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173267159-C-T

159087334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173266659-A-T

159087518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173266487-C-T

159087523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173266482-T-G

159088012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

159088117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -G-A

159088117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -G-T

159088345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -G-C

159088377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

159089004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173265670-C-G

159089089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173265603-T-A

159089202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173265471-T-A

159089798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173264949-A-G

159089885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173264860-T-C

159090002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173264762-T-C

159090132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173264655-C-T

159090186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173264592-C-G

159090260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173264534-C-T

159090356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173264443-C-T

http://identifiers.org/hco/1/GRCh38#159090480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173264329-C-A

159094775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173262655-C-T

159094904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173262517-T-C

159095371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173262060-G-A

159095398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173262032-C-G

http://identifiers.org/hco/1/GRCh38#159095487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173261966-A-C

159095531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173261921-T-C

159095544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173261908-A-G

159095611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173261829-T-C

159095738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173261687-T-C

159095924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173261490-T-G

http://identifiers.org/hco/1/GRCh38#159095967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173261311-C-A

159096025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173261251-C-T

http://identifiers.org/hco/1/GRCh38#159096086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173261213-A-C

159096099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173261201-G-A

159096332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173260884-A-T

159096840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173260388-A-G

159096884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173260339-G-A

159097053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173260152-C-T

159097201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173260032-A-G

159097247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173259992-A-G

159097746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173259591-T-C

159097849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173259476-C-T

159097865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173259460-C-T

159097866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173259459-C-G

159097866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173259459-C-T

159100734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173253699-G-C

159100734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173253699-G-T

http://identifiers.org/hco/1/GRCh38#159101042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173253426-A-C

http://identifiers.org/hco/1/GRCh38#159103404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173253357-A-C

159103404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173253357-A-T

http://identifiers.org/hco/1/GRCh38#159103507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173253258-A-C

159103862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173252879-G-A

159103862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173252879-G-C

159104229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173252498-G-A

http://identifiers.org/hco/1/GRCh38#159104233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173252494-C-A

159104233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173252494-C-T

159104260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173252467-A-G

159104264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173252463-T-C

159106559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173251269-G-T

159106724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173251139-A-G

159106805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173251078-T-C

159106943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173250961-T-C

http://identifiers.org/hco/1/GRCh38#159107107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173250808-A-C

159107136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173250779-T-G

159107334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173250603-G-A

159107334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173250603-G-T

159111373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173250485-G-A

159111614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173250260-T-C

159113524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173247312-G-C

159117299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173243615-G-T

159117363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173243554-T-C

159117696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173243257-T-C

159118069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173242896-T-A

159118069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173242896-T-C

159118102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173242854-C-T

159118148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173242814-T-C

159118174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173242785-T-G

159118188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173242771-G-A

159118879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173241850-G-A

159118895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173241835-T-C

http://identifiers.org/hco/1/GRCh38#159119040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173241711-A-C

159119130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173241619-C-T

http://identifiers.org/hco/1/GRCh38#159121043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173239463-C-A

159121043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173239463-C-T

159121708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173238790-G-T

159122316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 173238212-T-C

159122610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173237884-G-A

http://identifiers.org/hco/1/GRCh38#159122904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173237663-A-C

159123072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173237508-C-T

http://identifiers.org/hco/1/GRCh38#159123257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173237348-A-C

159123433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173237190-A-G

http://identifiers.org/hco/1/GRCh38#159123439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173237184-C-A

159123483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173237135-G-A

159123632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173236976-G-T

159123638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173236966-G-T

159123659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173236945-T-C

http://identifiers.org/hco/1/GRCh38#159123713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173236896-C-A

159124740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173235133-C-T

159124786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173235087-G-C

159124824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173235056-T-C

159124832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173235048-G-A

http://identifiers.org/hco/1/GRCh38#159125112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173232613-A-C

159125112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173232613-A-G

159125503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173232194-A-G

159125503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173232194-A-T

159125584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173232129-G-A

http://identifiers.org/hco/1/GRCh38#159125822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173231930-A-C

159125827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173231925-C-T

159125911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173231826-T-A

159126260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173231467-A-G

159126285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173231442-A-G

159127365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173230219-G-C

159130222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173228947-A-G

159130388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173228787-C-T

159130442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173228733-T-C

159130599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173228600-G-A

159130725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173228487-C-T

http://identifiers.org/hco/1/GRCh38#159130849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173228248-C-A

159131002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173228105-A-G

159131174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173227978-T-C

159131388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173227812-T-G

http://identifiers.org/hco/1/GRCh38#159131537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173227658-C-A

159131537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173227658-C-T

159131582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173226880-G-C

159131625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173226836-G-T

159131626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173226835-A-G

159131752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173226723-T-C

159132008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173226485-A-G

159132457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173226391-G-C

159132457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173226391-G-T

http://identifiers.org/hco/1/GRCh38#159132517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173226337-A-C

159132517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173226337-A-T

159132594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173226281-T-C

159132597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173226278-T-C

159132602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173226273-T-A

159132602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173226273-T-C

159132678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173226211-A-T

159133077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173225877-G-A

159133128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173225819-T-C

159133145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173225802-T-A

159133195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173225757-C-T

159133503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173225328-T-C

159133533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173225296-C-T

159134884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173224390-T-C

159135021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173224252-A-G

159135119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173224159-T-C

159135620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173223606-G-T

159135739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173223483-C-T

159135896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173223334-T-A

159136105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173223135-C-T

159136285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173222977-T-C

159136409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173222849-G-A

159136465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173222797-G-A

159136484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173222778-C-T

159136593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173222684-C-T

159136627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173222634-A-G

159136723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173222517-T-C

159136982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173222412-G-C

159137234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173222176-A-G

159138114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173221910-T-A

159138391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173221724-A-G

http://identifiers.org/hco/1/GRCh38#159138453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173221662-A-C

159138474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173221637-T-C

159138575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173221553-G-A

159138696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173221427-G-A

159138708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173221415-C-G

http://identifiers.org/hco/1/GRCh38#159138802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173221321-A-C

159138802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173221321-A-G

159138895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173221229-G-A

159138969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173220461-T-C

159139004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173220426-G-A

159139012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173220418-T-C

159139127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173220313-G-A

159139388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173220072-T-C

159139595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173219883-A-G

159140292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173219210-G-T

159140450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173219059-A-G

159140451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 173219058-A-G

159140464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173219045-A-G

159140481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173219031-A-G

159140593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173218915-T-C

159140631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173218877-C-T

159141261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173218283-G-A

159141280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173218264-G-A

159141280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173218264-G-C

159141280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173218264-G-T

159141284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173218244-G-A

159141391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173218151-A-G

159141526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173218050-C-G

159142245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173217306-A-G

http://identifiers.org/hco/1/GRCh38#159142320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173217232-A-C

http://identifiers.org/hco/1/GRCh38#159142830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173216685-C-A

159142911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173216611-G-A

159142911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173216611-G-T

159142930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173216591-A-T

159143319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173216237-A-G

159143321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173216235-G-A

159143398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173216149-C-G

159143509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173216045-G-T

159143613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173215907-C-T

159143714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173215832-A-G

http://identifiers.org/hco/1/GRCh38#159143887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173215710-A-C

159143949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173215656-A-G

159144062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173215550-A-G

159144133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173215498-G-A

http://identifiers.org/hco/1/GRCh38#159144288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173215385-A-C

159144288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173215385-A-G

159144326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173215348-A-G

http://identifiers.org/hco/1/GRCh38#159144401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173215296-C-A

159144494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173215215-A-T

159144625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173215081-C-T

159144741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173214963-T-C

159145198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173214501-A-T

159145266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173214433-C-T

159145474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173214229-A-T

159145510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173214194-A-G

http://identifiers.org/hco/1/GRCh38#159145530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173214174-C-A

159145530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173214174-C-T

159145690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173214009-G-A

159145701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173213998-C-G

159145701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173213998-C-T

159146225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173213812-T-A

159146225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173213812-T-C

159146225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173213812-T-G

159146233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173213805-C-T

159148038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173213114-G-A

159148042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173213110-G-T

159148198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173213028-T-C

159148227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173213000-T-C

159148252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173212973-A-G

159151239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173212662-T-C

http://identifiers.org/hco/1/GRCh38#159151299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173212600-C-A

159151376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173212520-C-T

159151534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173212356-T-C

159151648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173212244-T-A

159152353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173211862-A-G

159152479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173211737-T-C

159156958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173209446-T-C

159157030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173209370-T-C

http://identifiers.org/hco/1/GRCh38#159157031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173209369-C-A

159157031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173209369-C-T

http://identifiers.org/hco/1/GRCh38#159157356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173209052-C-A

159157469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173208952-C-T

159157491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173208925-T-C

159157504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173208912-T-A

159157733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173208809-T-C

159157782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173208779-T-G

159157899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173208692-A-G

159158413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173208201-T-G

159158746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173207619-G-A

159159956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173206252-C-T

159160367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173205732-T-C

159160413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173205687-A-G

159161175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173205271-T-C

159161236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173205208-G-A

159161236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173205208-G-C

159161564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173204888-T-C

159161590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173204863-A-T

159161596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173204857-C-T

159161848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173204646-A-T

159161889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173204602-G-A

159161897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173204594-C-T

http://identifiers.org/hco/1/GRCh38#159162136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173204368-A-C

159162353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173204153-G-A

159162425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173204104-C-T

159162474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173204054-G-A

159162481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173204044-T-G

http://identifiers.org/hco/1/GRCh38#159162694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#173203843-C-A

159162824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173203689-A-G

159163035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173203486-T-G

159163060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173203461-G-A

http://identifiers.org/hco/1/GRCh38#159163260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173203063-C-A

159163260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173203063-C-T

http://identifiers.org/hco/1/GRCh38#159163289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173202928-A-C

159163561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173202671-A-G

http://identifiers.org/hco/1/GRCh38#159163617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173202615-A-C

159163617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173202615-A-G

159163681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173202557-G-A

159163766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173202506-T-C

159163969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173202362-T-A

159164281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173202076-C-T

http://identifiers.org/hco/1/GRCh38#159164350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173202011-C-A

159164438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173201927-A-G

159164736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173201645-C-G

http://identifiers.org/hco/1/GRCh38#159165731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173200871-C-A

159165963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173200538-A-T

159166453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173200053-T-A

159167652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173198889-G-C

159167708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173198833-A-G

159167709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173198832-C-T

159167897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173198649-C-T

159168119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173198432-G-A

159168332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173198220-C-T

159168451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173198099-T-C

159168463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173198086-C-G

159168674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173197874-A-G

159168777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173197778-T-G

http://identifiers.org/hco/1/GRCh38#159168905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173197644-C-A

159168935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173197607-A-G

159168936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173197606-T-C

http://identifiers.org/hco/1/GRCh38#159169295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173197240-A-C

159169367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173197181-C-G

159169508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173197010-C-T

159169522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173196996-C-T

159169550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173196968-C-T

159169649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173196875-G-A

159169968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173196573-C-T

159170765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173195860-A-G

159171227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173195599-G-T

159171379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173195449-C-T

159171434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173195394-C-T

159171664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 173195162-G-A

159171931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173194899-A-G

http://identifiers.org/hco/1/GRCh38#159171973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173194856-A-C

159171973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173194856-A-G

http://identifiers.org/hco/1/GRCh38#159172723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173194116-C-A

159172775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173194053-G-A

159172775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173194053-G-C

159173593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173193249-G-A

159173593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173193249-G-T

159173688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173193153-C-G

159173796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173193049-C-T

159173822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173193022-C-T

159174242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173192685-A-G

159174341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173192610-C-T

159174524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173192431-G-A

http://identifiers.org/hco/1/GRCh38#159174580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173192375-A-C

159174963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173191993-A-G

159174964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173191992-A-G

159175224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173191730-T-C

159175242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173191712-T-C

159175275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173191679-C-G

159175341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173191613-G-A

159175341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173191613-G-T

159175342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173191612-T-C

159175356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173191598-G-T

http://identifiers.org/hco/1/GRCh38#159176415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173190402-A-C

159176415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173190402-A-G

http://identifiers.org/hco/1/GRCh38#159176471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173190340-A-C

159176868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173189962-G-A

159176868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173189962-G-T

159177082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173189751-G-C

159177671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 173189263-A-G

159177823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173189152-T-G

http://identifiers.org/hco/1/GRCh38#159178272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173189060-A-C

159178273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173189059-A-G

159178369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173188965-T-C

http://identifiers.org/hco/1/GRCh38#159178440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173188893-C-A

http://identifiers.org/hco/1/GRCh38#159178594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173188842-C-A

159178594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173188842-C-G

159179101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173188407-A-G

159179509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173188042-T-C

http://identifiers.org/hco/1/GRCh38#159179530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173188021-C-A

159179592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173187959-C-T

159179773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173187678-A-G

159180954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173186459-C-T

159181753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173185559-G-T

http://identifiers.org/hco/1/GRCh38#159182194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173185053-C-A

159182194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173185053-C-T

159182221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173185039-G-A

http://identifiers.org/hco/1/GRCh38#159182782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173184409-C-A

159182982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173184167-A-G

159183611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173183596-T-A

159183612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173183595-C-T

http://identifiers.org/hco/1/GRCh38#159184260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173182970-A-C

159184581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173182465-G-C

159184849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173182189-T-C

159185015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173181837-T-C

159185268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173181547-T-C

159185308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173181510-T-C

159185433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173181387-G-C

159185936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173180918-A-T

http://identifiers.org/hco/1/GRCh38#159185953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173180901-A-C

159186709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173179493-T-C

159186776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173179429-T-C

159187053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173179137-G-C

159187325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173178911-T-G

http://identifiers.org/hco/1/GRCh38#159187339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#173178897-C-A

159187384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173178842-C-T

159187544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173178672-G-A

159187544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173178672-G-C

159187712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173178511-C-T

159187767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173178462-T-C

159187775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 357
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 173178454-C-T