159157519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44456236-T-A

159157616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44456137-C-T

http://identifiers.org/hco/5/GRCh38#159157973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44455781-C-A

159157973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44455781-C-G

159157973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44455781-C-T

http://identifiers.org/hco/5/GRCh38#159158031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44455723-C-A

159158031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44455723-C-G

159158053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44455702-C-G

159158053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44455702-C-T

159158187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44455566-G-C

http://identifiers.org/hco/5/GRCh38#159158253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44455512-C-A

159158283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44455482-G-T

159158297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44455468-A-T

159158308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44455457-A-T

159158479-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44455294-C-G

159158479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44455294-C-T

http://identifiers.org/hco/5/GRCh38#159158550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44455225-C-A

159158551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44455224-T-C

http://identifiers.org/hco/5/GRCh38#159158591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44455182-C-A

159158591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44455182-C-T

159158614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44455159-A-T

159158668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44455112-C-T

159158674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44455106-G-A

159158674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44455106-G-T

159158749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44455031-T-C

159158756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 44455024-G-A

159158756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44455024-G-C

159158813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44454967-T-C

159158813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44454967-T-G

http://identifiers.org/hco/5/GRCh38#159158824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44454956-C-A

159158824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44454956-C-T

159158870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44454910-C-T

159159074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44454705-T-C

http://identifiers.org/hco/5/GRCh38#159159254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44454547-A-C

159159254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44454547-A-T

159159595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44454237-T-C

159159764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44454097-T-C

http://identifiers.org/hco/5/GRCh38#159159950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44453908-C-A

159160109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44453751-C-T

159160110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44453750-G-A

159160110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44453750-G-T

159160561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44453356-T-A

159160795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44453113-C-T

159160938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44452993-C-T

159161103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44452812-G-A

159161140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44452771-G-A

159161140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44452771-G-T

http://identifiers.org/hco/5/GRCh38#159161213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44452697-C-A

159161213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44452697-C-G

159161213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44452697-C-T

159161279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44452633-G-A

159161279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44452633-G-T

159161288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44452624-T-A

159161288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44452624-T-C

159161288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44452624-T-G

159161489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44452423-C-T

159161516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44452396-C-T

159161856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44452143-C-T

159162042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44452025-C-T

159162104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451960-A-G

159162297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451759-T-A

159162363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451697-C-G

159162363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451697-C-T

159162733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451168-C-T

159162823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44451009-C-T

159162849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44450992-A-T

159162933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 44450943-T-C

159167539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44450313-A-G

159167728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44450168-A-G

159167897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44450002-G-A

159167897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44450002-G-C

159167907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44449992-G-C

159167990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44449931-A-G

159168245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44449314-T-C

159168818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44448314-T-C

159168839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44448294-G-A

159168839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44448294-G-C

159168839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44448294-G-T

http://identifiers.org/hco/5/GRCh38#159168845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44448288-A-C

159168858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44448278-T-A

159168858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44448278-T-C

159168858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44448278-T-G

159168912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 44448224-G-A

159169028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44448108-T-C

http://identifiers.org/hco/5/GRCh38#159169064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44448074-A-C

159169064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44448074-A-G

159169096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44448042-G-A

159169096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44448042-G-C

159169096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44448042-G-T

159169165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44447975-T-A

159169166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44447974-T-G

159169169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44447971-G-T

159169445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446317-G-A

http://identifiers.org/hco/5/GRCh38#159169663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44446119-C-A

159169663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446119-C-T

159169667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44446115-G-A

http://identifiers.org/hco/5/GRCh38#159169829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44445956-A-C

159169829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44445956-A-G

159169981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44445816-T-C

159172602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44444999-T-C

159173586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442934-T-A

159173664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442855-T-C

159173675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442844-T-A

159173675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442844-T-C

http://identifiers.org/hco/5/GRCh38#159173861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44442736-C-A

159173862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442735-T-G

159173880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44442719-G-T

159174211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44442425-T-C

159174259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44442396-T-C

159174272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44442386-T-A

159174279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44442380-G-A

159174279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44442380-G-C

159174279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44442380-G-T

159174696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44441810-T-C

159174829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44441677-T-C

159174865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44441643-T-C

159174975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44441526-T-C

159175663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44440648-A-T

http://identifiers.org/hco/5/GRCh38#159175865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44440450-C-A

159175873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44440442-C-T

159176046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44440310-T-C

159176197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44440160-T-C

http://identifiers.org/hco/5/GRCh38#159176298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44440067-A-C

159176774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: missense variant
orthologous variants: 44439682-A-G

http://identifiers.org/hco/5/GRCh38#159176912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44439397-C-A

159176912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44439397-C-T

159177026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44439175-G-A

159177201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44439006-C-T

159177223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44438984-C-T

159177324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44438881-T-C

159180266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44436064-T-C

159180276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44436059-C-T

http://identifiers.org/hco/5/GRCh38#159180462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44435934-A-C

159180472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44435923-C-T

159180720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44435683-T-C

159181296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, undefined
orthologous variants: 44435519-G-C

http://identifiers.org/hco/5/GRCh38#159181916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44433582-C-A

http://identifiers.org/hco/5/GRCh38#159181921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44433577-C-A

159181921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron variant
orthologous variants: 44433577-C-T

http://identifiers.org/hco/5/GRCh38#159182185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44433333-A-C

159182198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44433319-T-A

159182288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44433230-G-T

159182299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44433219-T-C

159182309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44433209-G-A

http://identifiers.org/hco/5/GRCh38#159182339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44433179-A-C

159182361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44433159-C-G

159182417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44433103-T-C

159182452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44433083-C-G

159182553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44432981-A-G

159182971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44432376-T-G

159183524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44431894-T-G

159183621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44431827-A-G

http://identifiers.org/hco/5/GRCh38#159184744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44430323-A-C

http://identifiers.org/hco/5/GRCh38#159184863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44430220-A-C

159184866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44430217-C-T

159185271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44429847-G-A

159185295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429819-G-A

159185590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429451-T-C

159185647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44429306-T-C

159186055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44428891-C-T

159186116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44428826-T-C

http://identifiers.org/hco/5/GRCh38#159186418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44428535-C-A

159186610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44428327-C-T

159188767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44427145-T-C

159188857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44427053-C-G

http://identifiers.org/hco/5/GRCh38#159188980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44426982-C-A

159188980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44426982-C-G

159188980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44426982-C-T

159189667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44426424-T-C

159189667-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44426424-T-G

159190784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44425303-T-C

159193196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44423830-T-C

159193346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44423703-A-G

159193437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44423626-C-T

159193440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44423623-G-A

159193692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44423422-G-A

159194153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44423017-C-T

159194269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422889-A-G

159194655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422335-T-C

159194667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422296-A-G

159194861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422070-T-C

159194862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422069-A-G

http://identifiers.org/hco/5/GRCh38#159194868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44422063-C-A

159194872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422059-T-A

159194872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422059-T-C

159194911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422047-T-G

159194915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44422043-A-G

159195218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421763-C-T

159195223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421758-T-C

159195306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421682-T-C

159195346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421644-C-G

159195346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421644-C-T

159195623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44421408-T-C

http://identifiers.org/hco/5/GRCh38#159195691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44421341-C-A

159198555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44420358-G-C

159201615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44418112-A-T

159201668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44418062-A-T

http://identifiers.org/hco/5/GRCh38#159201739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44417995-A-C

159201739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44417995-A-G

159201780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44417957-T-G

159202215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44417528-C-T

159203094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44416388-T-A

http://identifiers.org/hco/5/GRCh38#159203699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44415713-A-C

159203713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415699-G-C

159203713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415699-G-T

http://identifiers.org/hco/5/GRCh38#159203743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44415669-A-C

159203743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415669-A-T

159203804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415645-G-A

159203804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415645-G-C

159204139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415352-A-G

159204239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415308-T-G

159204255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415293-G-A

159204269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44415283-T-C

159205065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44414661-T-C

159205103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44414625-C-T

http://identifiers.org/hco/5/GRCh38#159205388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44414350-C-A

159205869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44413574-T-A

159205938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44413524-A-G

159206081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44413371-A-G

http://identifiers.org/hco/5/GRCh38#159206131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44413347-C-A

159206131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44413347-C-G

159206131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44413347-C-T

159206354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412957-T-C

159206443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412864-G-A

159206443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412864-G-C

159206550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412762-T-C

159206676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412492-A-G

http://identifiers.org/hco/5/GRCh38#159206776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44412415-A-C

159206834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412358-T-C

159207162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44412041-G-A

http://identifiers.org/hco/5/GRCh38#159207406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#44411827-C-A

159207406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44411827-C-T

159207488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44411764-C-G

159207492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44411760-C-T

159207752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44411466-T-C

159207752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44411466-T-G

159207827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44411388-A-G

159207830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44411385-C-G

159207841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44411373-G-A

159207841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44411373-G-C

http://identifiers.org/hco/5/GRCh38#159207915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#44411296-C-A

http://identifiers.org/hco/5/GRCh38#159207974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44411238-C-A

159208088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44411122-G-A

159208088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44411122-G-T

159208539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44410705-T-A

159208539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44410705-T-C

http://identifiers.org/hco/5/GRCh38#159208584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#44410662-C-A

159208900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410347-A-G

159209028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410248-G-C

159209151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44410168-G-A

159209151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44410168-G-T

159209165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44410154-G-A

159209165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44410154-G-C

159209165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44410154-G-T

159209259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410071-G-A

159209259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410071-G-T

159209264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410066-G-A

159209264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410066-G-T

http://identifiers.org/hco/5/GRCh38#159209265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44410065-C-A

159209265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410065-C-G

159209265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44410065-C-T

http://identifiers.org/hco/5/GRCh38#159209350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#44409975-C-A

159209350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409975-C-G

159209350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409975-C-T

159209398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409927-G-A

159209398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409927-G-T

http://identifiers.org/hco/5/GRCh38#159209492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44409846-C-A

http://identifiers.org/hco/5/GRCh38#159209493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#44409845-C-A

159209493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44409845-C-G

159209493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44409845-C-T

159209575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409761-G-A

159209575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409761-G-T

http://identifiers.org/hco/5/GRCh38#159209666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#44409677-C-A

159209666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409677-C-T

http://identifiers.org/hco/5/GRCh38#159209678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#44409665-C-A

159209678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409665-C-T

http://identifiers.org/hco/5/GRCh38#159209722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#44409628-C-A

159209722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 44409628-C-G

159209740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44409610-G-A

159209948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20853
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 44409416-A-G