125315172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 5 prime UTR variant
orthologous variants: 38940047-C-G

125315280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 5 prime UTR variant
orthologous variants: 38940132-C-T

125315707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 5 prime UTR variant
orthologous variants: 38940536-G-A

125315715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 5 prime UTR variant
orthologous variants: 38940544-G-T

125315900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 38940660-C-T

125316226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38940941-T-A

http://identifiers.org/hco/4/GRCh38#125316259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38940973-C-A

125316259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38940973-C-G

125316295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 38941001-G-A

http://identifiers.org/hco/4/GRCh38#125316351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38941050-A-C

125316672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38941369-C-T

125316926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant
orthologous variants: 38941623-G-T

125317803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant
orthologous variants: 38942500-T-A

125318022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38942719-T-C

125318151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38942848-A-G

125318170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant
orthologous variants: 38942867-G-A

125318761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant
orthologous variants: 38943458-T-A

125318761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 38943458-T-C

http://identifiers.org/hco/4/GRCh38#125318826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38943523-C-A

125318826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38943523-C-G

125318826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38943523-C-T

125318917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38943614-A-G

125319186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38943883-T-G

http://identifiers.org/hco/4/GRCh38#125319337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38944034-C-A

125319337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38944034-C-T

http://identifiers.org/hco/4/GRCh38#125319513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38944210-C-A

125319513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38944210-C-T

125319696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38944393-T-C

125319762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38944459-G-A

125320002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38944699-T-A

125320035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38944732-C-G

125320035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38944732-C-T

http://identifiers.org/hco/4/GRCh38#125320071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38944768-A-C

125320170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38944867-T-C

125320182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38944879-G-C

125320248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38944945-T-C

125320281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38944978-A-G

125320321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38945018-G-A

125320734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38945431-A-G

125320827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38945524-T-A

125320853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38945550-A-G

125320911-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38945608-T-A

125321004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38945701-A-G

125321136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38945833-C-T

125321196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38945893-G-C

125321265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38945962-C-T

125321328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 38946025-G-T

125321514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38946211-A-G

125321541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 38946238-T-C

http://identifiers.org/hco/4/GRCh38#125321644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38946335-C-A

125321644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38946335-C-T

125321943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38946636-G-A

125321988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38946682-G-T

125322043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38946733-C-T

http://identifiers.org/hco/4/GRCh38#125322289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38946976-C-A

125322294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38946981-C-T

http://identifiers.org/hco/4/GRCh38#125322370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38947029-C-A

125322389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38947045-G-A

125322394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38947050-T-C

125322544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38947210-C-T

125322947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38947608-A-G

125323258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38947867-T-G

125323322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38947931-A-G

125323348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38947957-T-C

125323461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38948078-A-G

125323851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38948815-A-G

125323854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38948818-C-T

125323879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38948842-C-T

http://identifiers.org/hco/4/GRCh38#125323933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38948894-C-A

125323933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38948894-C-T

125324054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38949001-A-T

http://identifiers.org/hco/4/GRCh38#125324380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38949204-C-A

125324618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38949432-G-A

125327092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38953620-G-T

125327109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38953637-A-G

125327198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38953700-G-A

125327305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38953812-G-T

125327451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38954053-T-C

125327559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38954146-A-T

125327568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38954165-A-G

http://identifiers.org/hco/4/GRCh38#125327610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38954207-A-C

125327610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38954207-A-G

125327623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38954220-T-G

125327637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38954234-A-G

125327726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38954309-A-T

125327759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38954342-T-C

125327763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38954346-G-T

125327839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38954424-A-G

125333940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38955175-G-A

125333940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38955175-G-T

125333993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38955225-T-C

125334071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38955295-G-A

http://identifiers.org/hco/4/GRCh38#125334319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38955478-A-C

125334362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38955514-C-T

125334636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38955747-G-A

125334645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38955756-A-G

125334645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38955756-A-T

125334669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38955780-T-C

125334749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38955865-G-A

125334813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38955924-T-C

125334954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38956069-T-C

125335039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38956158-G-C

125335202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38956325-G-C

http://identifiers.org/hco/4/GRCh38#125335215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38956338-C-A

125335215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38956338-C-G

125335342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38956454-T-G

125335349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38956461-G-A

125335440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38956558-A-G

125335492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38956739-A-G

125335608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38956898-C-G

125335686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38956970-G-A

125335769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38957064-T-G

125335912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38957372-T-C

http://identifiers.org/hco/4/GRCh38#125336376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38957818-C-A

125336575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38957996-T-C

125336700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38958104-G-T

125336831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38958204-T-C

125336896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38958269-A-G

125337060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38958471-C-T

125337191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38958599-A-G

125337191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38958599-A-T

125337235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38958653-T-A

125337299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38958721-C-T

125337311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38958733-A-G

125337373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38958894-A-G

125337508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38959029-A-G

125337614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 38959124-G-A

125338126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38959749-T-A

125338126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38959749-T-C

125338126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38959749-T-G

125338139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38959762-G-A

125338152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38959775-G-A

125338251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38959863-G-T

125339034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38960865-T-C

125339583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38961091-A-G

125339627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38961135-C-G

125339627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38961135-C-T

125340357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38961793-T-A

125340400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38961846-T-A

125341357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38962656-A-G

125341406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38962715-G-A

125341491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38962804-G-A

125341550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38962850-G-A

125341584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 38962884-T-G

125342004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38963286-C-T

125342008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38963290-G-A

125342196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38963481-C-G

125342344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38963624-G-A

125342350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38963630-A-G

125342350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38963630-A-T

125343698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38965236-C-T

http://identifiers.org/hco/4/GRCh38#125343710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38965247-A-C

125343781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38965324-C-T

125343939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38965484-G-A

125343967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38965506-G-A

125344203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38965725-A-G

125344234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38965750-C-T

125344266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38965781-C-T

125344336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38965847-G-A

125344360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38965876-G-A

125344770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38966159-A-G

125345414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38966671-A-G

125345426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38966683-T-A

125345635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38966913-T-C

125346753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38968022-C-T

125347026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38968284-C-T

125348003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38970681-A-G

http://identifiers.org/hco/4/GRCh38#125348034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38970710-A-C

125348253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38970938-A-G

125348267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38970963-A-T

125348275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38970982-A-G

125348729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38971381-T-C

125348925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38971540-A-G

125348941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38971556-G-A

125349142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38971846-T-C

125349258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38971946-T-C

125349622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38972201-A-G

125349985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38972601-A-G

125349998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38972614-T-C

125350606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38973273-G-A

125350901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38973550-A-G

125350933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38973583-G-C

125351573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38974204-C-T

125351985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38974613-G-A

125352041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38974668-G-T

125352762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38974941-C-T

125353362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38975499-G-T

125353717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38975786-T-C

125353736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38975804-T-A

125353736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38975804-T-C

125353885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38975942-C-T

125354504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38976455-C-G

http://identifiers.org/hco/4/GRCh38#125354525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38976481-A-C

125354525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38976481-A-T

125355651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38977026-A-G

125355681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38977054-T-G

125355753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38977120-A-G

125355855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38977221-T-C

125355918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38977313-A-G

http://identifiers.org/hco/4/GRCh38#125356173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38977531-A-C

125356509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38977855-T-G

125356518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38977860-A-T

125356550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38977881-T-G

125356580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38977911-A-T

125356679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38978214-G-A

http://identifiers.org/hco/4/GRCh38#125356685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38978220-C-A

125356706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38978239-T-G

http://identifiers.org/hco/4/GRCh38#125356751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38978289-C-A

125356774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38978323-A-G

125356862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38978405-A-T

125357184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38978675-G-A

http://identifiers.org/hco/4/GRCh38#125357239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38978728-A-C

125357615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38979102-T-G

125357618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38979105-T-C

125357618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38979105-T-G

125357776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38979218-C-T

125357797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38979237-T-C

125357854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38979292-T-C

125358021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38979425-C-G

125358040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38979450-G-A

125360056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38979852-T-C

125361456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38980421-T-C

125361456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38980421-T-G

125361519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38980480-C-T

125361715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38981062-G-A

125367910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38982104-A-G

125368023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38982209-T-A

http://identifiers.org/hco/4/GRCh38#125368034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38982220-C-A

http://identifiers.org/hco/4/GRCh38#125368208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38982439-A-C

125368482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38982711-T-C

125368482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38982711-T-G

125368541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38982755-A-T

125368777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38982983-C-T

125368879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38983085-A-T

125368956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38983156-C-T

125368985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38983184-C-G

125369210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38983431-T-C

125369531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38983736-C-T

125369728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38983937-T-C

125369781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38983983-C-G

125369781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38983983-C-T

125369899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38984070-T-C

125369900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38984071-A-G

125369905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38984076-G-A

125369905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38984076-G-C

125370113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38984276-A-T

125388348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38988595-T-C

125388577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38988827-C-T

125388617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38988868-A-G

125388626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38988877-C-T

125388628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38988879-T-A

125388696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38988946-C-T

125388968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, undefined
orthologous variants: 38989213-G-A

125389307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38989544-G-A

125389307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38989544-G-T

125389407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38989630-T-C

125389448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38989672-A-T

125389643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38990537-T-C

125389699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, undefined
orthologous variants: 38990579-T-C

http://identifiers.org/hco/4/GRCh38#125389712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#38990595-C-A

125389726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, undefined
orthologous variants: 38990614-A-G

125389822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38990706-T-C

125390539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38991766-T-G

125390589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38991815-T-C

125390668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38991903-C-T

125390838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, undefined
orthologous variants: 38992029-T-C

125390865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, undefined
orthologous variants: 38992057-G-A

125391804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38992192-A-G

http://identifiers.org/hco/4/GRCh38#125391837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#38992223-A-C

125392212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38993175-T-C

125392294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38993260-A-G

125392363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38993321-G-T

125392393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38993349-A-G

125392394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38993350-T-G

125392412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38993363-G-C

125392441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38993392-C-G

125392498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38993441-T-C

125392709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38993629-G-A

125392778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38993792-T-G

125392779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38993793-G-T

125393074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38994074-G-T

125393217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38994211-G-A

125397288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38995620-G-A

125397423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38995738-G-T

125397448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38995763-C-T

125397662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38995946-A-G

125397830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38996107-C-T

125398077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38996334-C-T

125398286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38996521-G-A

125398286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38996521-G-T

125398383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38996619-A-G

125398496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38996702-G-A

125398689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38996878-G-A

125398689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38996878-G-T

125398724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38996914-T-A

125398724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38996914-T-C

125398733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38996923-T-C

125398765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38996939-G-T

125398852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 38997026-G-A

125398852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 38997026-G-C

125398852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 38997026-G-T

125399696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38998785-A-G

125399700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38998789-C-T

125400486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38999481-T-C

125400532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38999528-G-A

125400628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 38999664-G-A

125401034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39000040-A-T

125401102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39000091-C-T

125401245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39000236-A-G

125401861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39000815-A-G

http://identifiers.org/hco/4/GRCh38#125401867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39000821-C-A

125401867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39000821-C-T

125401960-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39000856-T-A

125401970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39000866-T-C

125402107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39000977-A-G

125402107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39000977-A-T

125402122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39000992-T-A

125402390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39001248-G-A

125402390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39001248-G-T

125402467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39001326-G-A

125406623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39003369-A-G

125406623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39003369-A-T

http://identifiers.org/hco/4/GRCh38#125406734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39003448-A-C

125406734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39003448-A-G

125406851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39003561-T-C

125406863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39003573-T-C

125406942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39003652-C-T

125406993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39003703-C-T

125407150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39003860-T-C

http://identifiers.org/hco/4/GRCh38#125407199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39003907-A-C

125407199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39003907-A-G

125407226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39003931-A-G

125407228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39003933-G-A

125407228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39003933-G-C

125407271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39003971-G-T

125407310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39004009-A-G

125407529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39004222-C-T

125407571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39004262-A-G

125407931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39004651-G-A

125407931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39004651-G-C

125407974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39004679-T-C

125408403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39005127-T-A

125408403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39005127-T-C

125408403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39005127-T-G

125408406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39005136-T-C

125408418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39005148-A-G

125408418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39005148-A-T

125408536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39005264-A-G

125408628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39005356-A-G

125408754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39005482-A-T

125408760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39005488-T-C

125408760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39005488-T-G

125408779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39005507-A-G

125408802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 39005530-T-C

125408837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39005565-T-C

125408875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39005609-G-T

125408929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39005666-A-G

125408929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39005666-A-T

125410765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39006800-G-A

125410815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39006850-A-G

125410978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39007025-A-T

125411176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39007203-T-C

http://identifiers.org/hco/4/GRCh38#125411235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39007260-A-C

125411860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39007887-A-G

125411995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39008019-G-T

125412399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39008361-T-C

125412433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39008395-G-C

125412806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39008659-T-C

125413138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39008860-T-G

http://identifiers.org/hco/4/GRCh38#125413270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39008941-A-C

125413270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39008941-A-G

125413773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39009433-G-A

125414227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39010055-A-G

http://identifiers.org/hco/4/GRCh38#125414231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39010059-C-A

125414718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39010539-T-C

125414848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39010784-A-G

125414850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39010786-G-A

125414850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39010786-G-T

http://identifiers.org/hco/4/GRCh38#125414895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39010833-C-A

125414954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39010892-T-C

125414954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39010892-T-G

http://identifiers.org/hco/4/GRCh38#125414985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39010923-C-A

125414985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39010923-C-G

125414985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39010923-C-T

http://identifiers.org/hco/4/GRCh38#125415033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39010971-C-A

125415074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39011012-C-T

125415128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39011066-A-T

http://identifiers.org/hco/4/GRCh38#125415134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39011072-A-C

125415134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39011072-A-G

125415272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39011210-T-C

125415398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39011336-T-C

125415521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39011459-T-C

125415626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39011564-G-A

125415626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39011564-G-T

125415698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39011636-C-T

125415795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39011733-A-G

125415795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39011733-A-T

http://identifiers.org/hco/4/GRCh38#125415863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39011801-A-C

125415863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39011801-A-G

125415863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39011801-A-T

http://identifiers.org/hco/4/GRCh38#125415865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39011803-C-A

125415865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39011803-C-T

http://identifiers.org/hco/4/GRCh38#125415878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39011816-C-A

125415878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39011816-C-T

125415880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39011818-G-A

125415882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39011820-G-A

http://identifiers.org/hco/4/GRCh38#125415927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39011868-C-A

125415927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39011868-C-G

125416036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39011935-G-A

125416097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39012001-A-G

125416159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39012054-G-A

125416159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39012054-G-C

125416165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39012060-C-G

125416214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39012101-T-G

125416226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39012113-C-T

125416245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39012132-T-C

125416292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39012178-T-C

125416385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39012397-G-A

125416385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39012397-G-T

http://identifiers.org/hco/4/GRCh38#125416405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39012452-C-A

125416405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39012452-C-G

125416405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39012452-C-T

125416530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39012632-C-G

125417156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39012912-A-G

125418016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39016055-A-G

125418319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39016362-G-A

125418363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39016407-T-C

125418469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39016501-A-T

125418477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39016509-C-G

125418670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39016676-G-A

125418684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39016716-A-G

125418856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39016886-C-T

125418864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39016894-A-G

125418926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39016953-C-T

125418960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39016982-G-C

125419086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39017093-C-T

125419146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39017165-A-G

125419239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39017286-G-C

125419287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39017313-A-G

125419287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39017313-A-T

125425478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39019045-G-A

125425541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39019108-A-G

125425925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39019415-A-G

125426122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39019617-T-G

125426221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39019713-A-T

125426325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39019799-C-T

125426389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39019854-T-C

125426389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39019854-T-G

125426392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39019857-C-T

125426401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39019866-A-G

125426452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39019945-G-T

125426476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39019987-G-C

125426561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39020077-T-C

125426582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39020087-T-C

http://identifiers.org/hco/4/GRCh38#125426611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39020116-A-C

125426648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39020146-A-G

125426776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39020263-C-T

125427117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39020495-C-G

125427117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39020495-C-T

125427219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39020593-T-G

125427691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39020983-G-A

125428376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39021430-G-T

125428396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39021443-A-G

125428414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39021461-A-G

125428551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39021489-T-A

http://identifiers.org/hco/4/GRCh38#125428879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39021786-C-A

125429593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39022427-T-C

125429656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39022493-G-T

125432654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39023260-A-G

125432657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39023263-G-A

125432809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39023374-A-G

125432833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39023414-A-G

http://identifiers.org/hco/4/GRCh38#125432991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39023582-A-C

125433008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39023591-A-G

125433012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39023595-T-A

125433136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39023713-T-A

125433143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39023723-A-G

125433321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39023902-A-T

125433596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39024172-C-G

125433621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39024195-C-T

125433747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39024293-C-T

125433854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39024395-T-A

125433893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39024445-G-C

125433900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39024451-T-C

http://identifiers.org/hco/4/GRCh38#125434079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39024635-A-C

125434166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39024694-T-C

125434221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39024751-G-C

125434300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39024830-T-C

125434346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39024876-C-T

125434358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39024888-C-T

http://identifiers.org/hco/4/GRCh38#125434393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39024923-A-C

125434443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39024973-T-G

http://identifiers.org/hco/4/GRCh38#125434519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39025038-C-A

http://identifiers.org/hco/4/GRCh38#125434596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39025105-C-A

125434600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39025109-T-C

125434662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39025291-G-A

125434684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39025319-C-T

125434726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39025361-A-G

125434769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39025390-C-T

125434860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39025473-T-C

125434922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39025516-A-G

http://identifiers.org/hco/4/GRCh38#125434974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39025567-A-C

125435119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39025683-G-A

125435288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39025839-G-A

125435360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39025898-G-A

http://identifiers.org/hco/4/GRCh38#125441351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39027952-A-C

125441351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39027952-A-G

125441371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39027972-A-G

125441427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39028020-A-G

125441548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39028164-T-C

http://identifiers.org/hco/4/GRCh38#125441567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39028183-C-A

125441665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39028276-G-C

125441719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39028309-C-T

http://identifiers.org/hco/4/GRCh38#125441731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39028321-C-A

http://identifiers.org/hco/4/GRCh38#125441807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39028400-A-C

125441808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39028401-G-T

125441822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39028415-G-T

125441882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39028474-A-G

125441884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39028476-T-C

125441884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39028476-T-G

125441977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39028564-C-T

125443432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39029045-T-C

125443599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39029211-G-A

125443793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39029372-G-C

125443893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39029468-A-G

125443893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39029468-A-T

125445251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39030401-A-G

125445259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39030409-A-G

125445413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39030553-G-A

125445575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39030689-C-T

125445787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39030898-A-G

http://identifiers.org/hco/4/GRCh38#125445970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39031080-A-C

http://identifiers.org/hco/4/GRCh38#125446109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39031233-A-C

125446109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39031233-A-G

http://identifiers.org/hco/4/GRCh38#125446204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39031318-C-A

http://identifiers.org/hco/4/GRCh38#125446225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39031340-A-C

125446225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39031340-A-G

125446262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39031387-G-T

125446273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39031398-A-G

125446402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39031525-G-C

http://identifiers.org/hco/4/GRCh38#125446592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39031859-C-A

http://identifiers.org/hco/4/GRCh38#125446596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39031863-C-A

125446610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39031877-T-C

125446621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39031893-T-C

125446626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39031899-C-T

125446741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39032022-A-T

125446821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39032110-A-G

125446837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39032126-T-G

125446888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39032177-G-A

http://identifiers.org/hco/4/GRCh38#125446951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39032355-A-C

125447028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39032449-A-G

125447578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39032963-C-T

125447627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033012-A-G

125447649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033036-T-C

125447665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033052-G-C

125448041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033420-G-A

125448041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033420-G-T

125448049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033428-A-G

125448130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033510-T-C

125448204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033567-G-A

125448312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033667-G-T

http://identifiers.org/hco/4/GRCh38#125448336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39033691-C-A

http://identifiers.org/hco/4/GRCh38#125448337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39033692-C-A

125448337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033692-C-T

http://identifiers.org/hco/4/GRCh38#125448392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39033736-C-A

http://identifiers.org/hco/4/GRCh38#125448404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39033753-A-C

125448433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033772-G-A

125448433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033772-G-C

http://identifiers.org/hco/4/GRCh38#125448439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39033778-C-A

125448439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033778-C-G

125448439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39033778-C-T

125448611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39033950-C-T

http://identifiers.org/hco/4/GRCh38#125448612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39033951-A-C

125448633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39033972-T-C

125448922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39034261-G-A

125448972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39034311-C-T

http://identifiers.org/hco/4/GRCh38#125448990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39034329-A-C

125449018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39034357-A-G

125449176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39034515-T-C

125449176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39034515-T-G

125449177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39034516-G-A

http://identifiers.org/hco/4/GRCh38#125449293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39034632-C-A

http://identifiers.org/hco/4/GRCh38#125449300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39034639-A-C

125449300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39034639-A-T

125449317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39034656-T-G

125449323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39034662-T-C

125449452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39034791-G-A

125449671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39035010-T-G

125449689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39035028-A-G

125449888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: stop gained
orthologous variants: 39035227-C-T

125449906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39035245-A-G

125450088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39035427-T-G

http://identifiers.org/hco/4/GRCh38#125450402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39035741-C-A

http://identifiers.org/hco/4/GRCh38#125450496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39035835-C-A

125450496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39035835-C-G

125450496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39035835-C-T

125450756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39036095-C-T

125450871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39036210-T-C

125450886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39036225-G-A

125450889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39036228-A-G

125450958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39036297-T-C

125451390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39036729-G-C

125451390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39036729-G-T

125451456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39036795-T-G

125451480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39036819-C-G

125451505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39036844-T-C

125451699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39037038-C-T

125451732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39037071-T-C

125451732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39037071-T-G

125451748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39037087-G-A

125451760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39037099-C-G

125451813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39037152-T-C

125451813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39037152-T-G

http://identifiers.org/hco/4/GRCh38#125451939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39037278-A-C

125451958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39037297-C-T

http://identifiers.org/hco/4/GRCh38#125452107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39037446-C-A

125452107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39037446-C-T

125452176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39037515-A-G

http://identifiers.org/hco/4/GRCh38#125452242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39037581-A-C

125452242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39037581-A-T

125452263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39037602-A-G

125452290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39037629-T-C

125452503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39037842-C-G

125452570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39037909-C-G

125452570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39037909-C-T

125452755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39038094-C-T

125452788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39038127-T-C

125452833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39038190-C-T

125458015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39040187-G-T

125458167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39040355-C-T

125458229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39040414-G-A

125458340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39040458-G-C

125458628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39040645-A-G

125459206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39041198-A-T

125459260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39041267-C-G

125459337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39041332-G-T

125459601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39041704-A-G

125459601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39041704-A-T

125459795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39041878-T-C

125460158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39042184-A-G

125460230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39042259-C-T

125461088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39042482-T-C

125461108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39042504-T-A

125461162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39042558-A-G

125461245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39042631-T-C

125461277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39042658-T-A

125461324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39042702-A-G

125461714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39043286-A-G

125461869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39043460-G-A

125461889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39043480-G-A

125461915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39043501-C-T

125462816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39045018-A-G

125462904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39045087-T-C

125462929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39045109-A-T

125463024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39045198-T-C

125463117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39045341-A-G

125463353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39045585-G-A

125463353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39045585-G-T

125463420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39045642-T-A

http://identifiers.org/hco/4/GRCh38#125463440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39045661-C-A

125463440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39045661-C-G

125463440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39045661-C-T

http://identifiers.org/hco/4/GRCh38#125463471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39045690-C-A

125463471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39045690-C-T

125463492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39045723-T-A

125463492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39045723-T-C

http://identifiers.org/hco/4/GRCh38#125463603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39045823-C-A

125463603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, missense_variant
orthologous variants: 39045823-C-G

125463603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 39045823-C-T

http://identifiers.org/hco/4/GRCh38#125463606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39045826-C-A

125463606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 39045826-C-G

125463787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39046093-T-C

125465098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39046670-A-G

125465600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39047103-G-A

http://identifiers.org/hco/4/GRCh38#125465642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39047133-A-C

125465642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39047133-A-G

125466009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39047498-T-C

125466322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39047782-A-G

125466460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39047919-T-G

125467230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39048539-G-A

125467305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39048618-T-C

125467399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39048712-G-A

125467493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39048805-T-A

125467564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39048873-G-C

http://identifiers.org/hco/4/GRCh38#125468431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39049972-A-C

http://identifiers.org/hco/4/GRCh38#125468451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39049991-A-C

125468451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39049991-A-G

125468477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39050018-A-G

125468504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 39050037-T-C

125468513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 39050046-T-A

125468513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 39050046-T-C

125468522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39050055-A-G

http://identifiers.org/hco/4/GRCh38#125468621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39050154-C-A

125468688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39050221-T-C

http://identifiers.org/hco/4/GRCh38#125468705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39050238-C-A

125468705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39050238-C-T

125468777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39050310-A-G

125468795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39050328-T-C

125468795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39050328-T-G

http://identifiers.org/hco/4/GRCh38#125468825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39050358-A-C

125468825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39050358-A-G

125473857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39050684-G-C

125473988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39050817-A-G

125474437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39051275-A-T

http://identifiers.org/hco/4/GRCh38#125474438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39051276-A-C

125474442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39051280-T-C

125474752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39051598-G-C

125474886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39051712-G-A

125475272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39052046-A-G

125475272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39052046-A-T

http://identifiers.org/hco/4/GRCh38#125475307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39052081-A-C

125475307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39052081-A-G

125475307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39052081-A-T

125475309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39052083-T-C

125475431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39052198-T-C

125475432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39052199-G-A

125475730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39052580-G-A

125476054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053104-G-A

125476080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053137-A-G

125476103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053158-T-C

125476110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053165-T-C

125476111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053166-G-A

125476111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053166-G-T

http://identifiers.org/hco/4/GRCh38#125476136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39053191-C-A

125476136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053191-C-T

125476137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053192-T-C

http://identifiers.org/hco/4/GRCh38#125476242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39053292-A-C

125476242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39053292-A-G

125476263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 39053313-A-G

125476267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053317-G-T

125476273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053322-G-A

http://identifiers.org/hco/4/GRCh38#125476319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39053460-C-A

125476319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053460-C-T

125476323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053464-A-G

125476338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053517-T-C

125476339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053518-G-A

125476339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053518-G-T

125476344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053531-G-A

125476344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053531-G-T

125476403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053613-G-A

125476403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053613-G-T

125476460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053674-G-C

125476478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053686-G-T

125476585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053793-T-C

125476700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053890-A-G

125476847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053982-A-T

125476860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053994-C-T

125476861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39053995-A-G

125476979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39054124-G-A

125476989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39054134-C-T

125477164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39054268-T-G

125477309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39054413-T-C

125479641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055161-T-A

125479641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055161-T-C

125479641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055161-T-G

125479668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055188-G-A

125479668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055188-G-C

125479668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055188-G-T

125479673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055193-T-C

125479673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055193-T-G

http://identifiers.org/hco/4/GRCh38#125479678-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39055195-A-C

125479678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055195-A-G

125479678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055195-A-T

125479712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055231-G-A

125479712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055231-G-T

http://identifiers.org/hco/4/GRCh38#125479723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39055240-C-A

125479723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055240-C-G

125479723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055240-C-T

http://identifiers.org/hco/4/GRCh38#125479771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39055292-C-A

125479771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 39055292-C-T

125479786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 39055307-T-C

125479792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 39055313-C-G

125479792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 39055313-C-T

http://identifiers.org/hco/4/GRCh38#125479887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39055408-C-A

125479887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055408-C-T

125479893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055414-G-T

125479924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055445-A-G

125479924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055445-A-T

http://identifiers.org/hco/4/GRCh38#125479928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39055449-A-C

125479945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055466-A-T

http://identifiers.org/hco/4/GRCh38#125479959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39055476-C-A

125479959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055476-C-T

http://identifiers.org/hco/4/GRCh38#125479984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39055502-A-C

125480001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055510-T-C

125480040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055547-G-T

125480064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055558-A-G

125480315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055783-T-A

125480440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39055907-C-T

125480566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39056039-G-A

125480950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39056390-C-T

125480955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39056393-A-G

125480962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39056400-T-G

http://identifiers.org/hco/4/GRCh38#125481086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39056485-C-A

125481086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39056485-C-T

125481179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39056585-G-T

125481238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39056638-T-C

125481264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39056664-T-C

125481264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39056664-T-G

125481399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39056800-G-A

125481399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39056800-G-T

125481433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39056823-T-C

125481466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39056856-T-G

125481693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39057082-C-T

125481723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39057112-T-G

125481755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39057144-T-C

125481769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39057163-G-C

125481769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39057163-G-T

http://identifiers.org/hco/4/GRCh38#125481783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39057180-C-A

http://identifiers.org/hco/4/GRCh38#125481854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39057249-A-C

http://identifiers.org/hco/4/GRCh38#125481871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39057266-C-A

125481894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39057289-C-G

125482001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39057406-T-C

http://identifiers.org/hco/4/GRCh38#125482068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39057475-C-A

125482068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39057475-C-T

125482192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39057570-C-T

125482283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39057676-A-G

125483011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39058672-G-A

125483011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39058672-G-T

125483065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39058732-G-A

125483438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39059180-A-G

125483473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39059215-A-G

125483744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39059436-A-G

125483744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39059436-A-T

125483838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39059520-A-G

125483846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39059528-A-G

125483870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39059554-G-T

125483968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39059632-T-C

http://identifiers.org/hco/4/GRCh38#125486360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39060296-A-C

http://identifiers.org/hco/4/GRCh38#125486420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39060356-A-C

125486420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39060356-A-G

125486804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39060705-G-T

125487141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39061040-G-A

125487161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39061060-A-G

125487213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39061111-T-A

http://identifiers.org/hco/4/GRCh38#125487255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39061152-C-A

125487255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39061152-C-G

125487374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39061270-C-T

125487527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39061423-G-C

125487723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39061643-T-A

125487723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39061643-T-G

125487767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39061684-T-C

125488120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39061957-C-G

125488173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39062005-T-C

125488285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39062067-T-C

125488342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39062124-C-T

125488502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39062282-G-A

125488657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39062417-A-G

125488657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39062417-A-T

125488694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39062453-T-A

125489396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39062663-G-A

http://identifiers.org/hco/4/GRCh38#125489630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39062919-A-C

125489647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39062929-T-C

125489752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39063020-T-A

125489756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39063024-G-T

125489801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39063044-A-G

125489801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39063044-A-T

http://identifiers.org/hco/4/GRCh38#125489831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39063075-C-A

125489831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: 39063075-C-T

http://identifiers.org/hco/4/GRCh38#125489832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39063076-A-C

125489895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 39063120-T-A

125489895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 39063120-T-C

125490013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39063239-C-G

125490157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39063383-G-A

125490157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39063383-G-T

125490211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39063437-G-C

http://identifiers.org/hco/4/GRCh38#125490273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39063499-C-A

125490279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39063505-G-T

125490284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39063510-G-A

125490334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39063560-T-C

125490469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39063695-G-A

125490517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39063743-T-C

125490706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39063932-C-T

125490748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39063974-C-G

125490805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: 39064031-G-C

http://identifiers.org/hco/4/GRCh38#125490910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39064139-C-A

125491111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39064340-T-C

125491111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39064340-T-G

125491213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39064442-A-G

125491411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: stop gained
orthologous variants: 39064640-T-A

125491411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39064640-T-C

125491450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39064679-T-C

http://identifiers.org/hco/4/GRCh38#125491534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39064763-C-A

125491534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39064763-C-T

125491735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39064958-C-T

125491762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: synonymous variant
orthologous variants: 39064985-T-C

125491841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 3 prime UTR variant
orthologous variants: 39065043-G-A

125491841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 3 prime UTR variant
orthologous variants: 39065043-G-T

125491845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 3 prime UTR variant
orthologous variants: 39065047-G-A

125491845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 3 prime UTR variant
orthologous variants: 39065047-G-T

http://identifiers.org/hco/4/GRCh38#125492067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39065266-A-C

125492067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 3 prime UTR variant
orthologous variants: 39065266-A-G

125492398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 3 prime UTR variant
orthologous variants: 39065587-G-A

http://identifiers.org/hco/4/GRCh38#125492689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23109
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#39065886-C-A