61187469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23439802-G-C

http://identifiers.org/hco/2/GRCh38#61187667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23439618-C-A

61187667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23439618-C-G

61187667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23439618-C-T

61187799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23439480-T-C

61188201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23439087-C-T

61188284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23439004-C-G

61188284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23439004-C-T

61188295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23438993-A-G

61188440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23438851-C-G

61188440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23438851-C-T

61188469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23438822-T-G

61188495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23438796-T-G

61188556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23438735-A-G

http://identifiers.org/hco/2/GRCh38#61188721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23438565-C-A

61188721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23438565-C-G

61188721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23438565-C-T

61188898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23438378-C-T

http://identifiers.org/hco/2/GRCh38#61189216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23438087-A-C

http://identifiers.org/hco/2/GRCh38#61189251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23438055-C-A

61189251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23438055-C-T

61189268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23438038-T-C

61189268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23438038-T-G

61189799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437752-G-A

61189849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437703-T-G

61189885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437682-A-G

61189925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437644-A-G

61189942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437633-T-G

61189951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437624-A-G

http://identifiers.org/hco/2/GRCh38#61189995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23437589-C-A

61189995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437589-C-G

61189995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437589-C-T

http://identifiers.org/hco/2/GRCh38#61190002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23437582-A-C

61190002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437582-A-G

61190002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437582-A-T

61190138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437338-G-A

61190138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437338-G-T

61190231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437249-A-G

61190245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437235-T-C

61190258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 23437233-G-A

61190436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23437032-A-T

http://identifiers.org/hco/2/GRCh38#61190450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23437014-C-A

http://identifiers.org/hco/2/GRCh38#61190453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23437011-C-A

61190453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23437011-C-G

61190982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23436422-A-G

http://identifiers.org/hco/2/GRCh38#61191043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23436356-C-A

61191047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23436352-T-C

61191306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23435805-G-T

61191461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23435700-G-A

61191461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23435700-G-C

61191485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23435676-A-G

61192395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23434456-T-G

61193122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23433946-T-C

61193127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23433941-T-A

61193170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23433893-T-A

http://identifiers.org/hco/2/GRCh38#61193220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23433836-C-A

61193237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23433819-A-G

61193334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23433733-G-A

61193334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23433733-G-T

61193426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23433655-T-C

61193523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23433578-G-A

61193523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23433578-G-C

61193559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23433544-C-G

http://identifiers.org/hco/2/GRCh38#61193567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23433507-A-C

61193567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23433507-A-G

61193591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23433427-T-C

61193674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23433352-C-T

61193932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23433118-G-T

http://identifiers.org/hco/2/GRCh38#61196891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23432241-C-A

61196891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23432241-C-G

61196891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23432241-C-T

61200528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23431070-A-G

61200719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23426423-G-T

61200744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23426417-T-A

61200857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23426277-T-C

http://identifiers.org/hco/2/GRCh38#61200916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23426245-A-C

http://identifiers.org/hco/2/GRCh38#61200998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23426173-A-C

61201430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425813-G-C

http://identifiers.org/hco/2/GRCh38#61202037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23425375-A-C

61202047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425365-A-G

61202246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425173-C-T

61202269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425151-G-T

61202285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425136-A-G

61202313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23425111-T-C

61202633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424906-G-A

61202635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424904-T-C

61202753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424804-G-A

61202771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424786-G-A

61202810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424747-C-T

61202846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424709-T-C

61202950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424606-C-T

61203435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23424092-T-C

http://identifiers.org/hco/2/GRCh38#61203598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23423948-C-A

61203598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23423948-C-T

61203806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23423727-G-C

61204636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422915-T-C

61204636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422915-T-G

61204654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422898-T-A

61204676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422876-C-T

61204814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422745-G-C

61204816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23422743-T-C

61205655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421941-A-G

61205967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421625-A-G

http://identifiers.org/hco/2/GRCh38#61205976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23421616-C-A

61205976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421616-C-T

http://identifiers.org/hco/2/GRCh38#61206166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23421437-A-C

61206177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23421426-C-G

61206360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420800-G-A

61206539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420641-C-T

http://identifiers.org/hco/2/GRCh38#61206620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23420546-C-A

http://identifiers.org/hco/2/GRCh38#61206648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23420519-C-A

61206648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420519-C-G

http://identifiers.org/hco/2/GRCh38#61206680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23420493-C-A

61206680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420493-C-G

61206708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420468-T-C

61206719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420457-T-C

61206719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23420457-T-G

http://identifiers.org/hco/2/GRCh38#61208572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23419101-C-A

61208624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23419047-T-C

http://identifiers.org/hco/2/GRCh38#61209112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23418681-C-A

http://identifiers.org/hco/2/GRCh38#61211492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23417625-C-A

61211492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417625-C-G

61211492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417625-C-T

http://identifiers.org/hco/2/GRCh38#61211518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23417601-C-A

61211518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417601-C-T

61211968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23417102-A-G

http://identifiers.org/hco/2/GRCh38#61212069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23416998-A-C

61213499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415989-G-A

61213502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415986-G-T

61213638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415873-G-A

61213638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415873-G-C

http://identifiers.org/hco/2/GRCh38#61213641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23415870-A-C

61213731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23415561-T-A

61215065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23413759-G-A

61219761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23411673-G-C

61219773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23411663-T-A

61219884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23411547-G-A

61221111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409686-G-C

61221269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23409537-T-C

61221755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23409005-T-A

61221755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23409005-T-C

http://identifiers.org/hco/2/GRCh38#61221774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23408983-C-A

61221774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23408983-C-T

61221842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23408913-G-T

61222097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23408662-T-G

61222127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23408643-G-C

61223255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23407837-C-G

61223552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23407533-G-A

61223552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23407533-G-C

61223552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23407533-G-T

61223703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23407450-T-C

61224149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23407125-G-C

61224607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23406676-C-T

61224874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23406401-C-T

61225701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23405883-G-A

61225748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23405833-T-C

61226313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23405446-T-C

61226867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23404822-A-G

61226900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23404789-G-A

61226900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 23404789-G-T

61227130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23404611-G-A

61228151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23403331-T-C

http://identifiers.org/hco/2/GRCh38#61228278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23403215-C-A

61228408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23403101-T-G

61228519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402988-T-C

61228523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402984-T-C

61228523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402984-T-G

61228609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402899-C-G

61228612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402897-C-G

http://identifiers.org/hco/2/GRCh38#61228804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23402708-A-C

61228903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23402609-C-G

61229033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402478-G-C

61229033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402478-G-T

61229051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402456-G-A

61229051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402456-G-T

61229125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402403-G-A

61229125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402403-G-T

61229536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23402091-A-T

61231950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399662-A-G

http://identifiers.org/hco/2/GRCh38#61232382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23399342-A-C

61232426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399302-T-A

61232426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399302-T-C

61232426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399302-T-G

61232554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399192-T-C

61232636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399111-T-G

61232652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23399092-A-G

61234184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23398451-G-A

61234291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23398354-C-T

61235674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23397168-T-G

61235937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23396885-T-C

61235966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23396857-A-T

61236154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23396659-T-C

61236278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23396536-T-A

61236281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23396533-T-A

61236281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23396533-T-C

61236305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23396511-A-G

61236306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23396510-T-A

61236306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23396510-T-G

61236307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23396509-G-A

61241430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23394505-T-A

61241430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23394505-T-C

61241520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23394438-C-G

61241702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23394258-A-G

61241825-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23394139-T-A

61241825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23394139-T-C

61241825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23394139-T-G

http://identifiers.org/hco/2/GRCh38#61241826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23394138-A-C

61241826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23394138-A-G

61242334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23393042-T-G

61242384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23392993-A-T

http://identifiers.org/hco/2/GRCh38#61242421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23392970-A-C

61242680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23392736-G-T

61245301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391085-A-G

61245321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391033-G-A

61245321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391033-G-T

http://identifiers.org/hco/2/GRCh38#61245331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23391023-A-C

61245331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391023-A-G

61245348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23391007-T-C

61245959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389914-T-C

61246180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389681-G-A

61246180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389681-G-C

61246180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389681-G-T

61246252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23389103-A-G

61246450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23388892-T-A

61246526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23388836-G-A

61248441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23386127-T-C

61248555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23386033-G-A

61248555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23386033-G-T

61248707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23385875-T-C

61255352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23383926-C-G

61255590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23383673-T-G

61256224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23383473-C-T

61256279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23383424-T-C

61256405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23383251-T-G

61256497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23383159-T-A

61256497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23383159-T-C

61256590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23383056-T-A

61256590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23383056-T-G

61256833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23382786-A-G

61256835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23382784-A-G

61257034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23382547-A-G

61257211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 23382383-G-A

61257487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23381799-T-C

61259754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 23379320-T-C

61259763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 23379311-A-G

http://identifiers.org/hco/2/GRCh38#61259786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23379288-A-C

61259823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379260-G-T

61259889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379218-T-A

http://identifiers.org/hco/2/GRCh38#61259904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23379204-C-A

61259904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379204-C-G

61259904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379204-C-T

61260041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23379023-G-A

61260220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23378759-A-G

61260220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23378759-A-T

61260221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23378758-A-G

http://identifiers.org/hco/2/GRCh38#61265162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23376993-C-A

61265301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23376885-T-A

61265301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23376885-T-C

http://identifiers.org/hco/2/GRCh38#61265326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23376849-A-C

61265349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23376826-T-C

61265391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23376799-T-C

61265790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23376422-G-T

61266001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23376226-A-G

61266031-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23376196-T-G

61266076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23376151-G-A

61266076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 23376151-G-C

61266187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23376035-A-G

61266187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23376035-A-T

61266258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23375966-T-C

http://identifiers.org/hco/2/GRCh38#61266268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23375945-C-A

61266268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23375945-C-G

61266268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23375945-C-T

http://identifiers.org/hco/2/GRCh38#61266281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23375932-C-A

61266335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23375891-A-G

61276998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23371924-G-A

61278455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23371084-A-G

http://identifiers.org/hco/2/GRCh38#61278548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23370992-C-A

61278548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23370992-C-T

61280169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23370215-A-G

61280366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23370021-T-C

61280462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369937-T-A

61280670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369480-T-C

61280749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369410-A-G

61280986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369226-A-G

61281000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369197-A-T

61281013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369184-G-C

61281013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369184-G-T

61281037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23369163-G-A

61281249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 23368970-G-A

61287063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23363804-G-A

61287277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23363594-G-T

61287375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23363492-A-G

61287471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23363393-G-C

61287477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23363387-A-G

61288199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 23362886-C-T

http://identifiers.org/hco/2/GRCh38#61288306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23362786-C-A

61288306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23362786-C-T

61288535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23362563-T-C

61288535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23362563-T-G

61288585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23362517-A-T

61288639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23362457-A-G

http://identifiers.org/hco/2/GRCh38#61288650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23362446-C-A

61288650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23362446-C-G

61288907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23362180-T-C

61289381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23360292-C-G

61289381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23360292-C-T

61289515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23360193-G-A

61289791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23359913-T-C

61289807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23359899-C-T

61289839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23359866-G-A

61293626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23355784-G-A

61293626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23355784-G-T

61294899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353940-T-A

61294899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353940-T-C

61294899-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353940-T-G

61294913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353929-T-G

61295071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353768-A-G

61295075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353764-A-T

61295100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353740-A-G

61295128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353718-G-A

61295265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 23353583-T-C

61295386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353459-T-C

61295429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353419-G-A

61295429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353419-G-C

61295429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353419-G-T

61295436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353412-A-G

61295436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23353412-A-T

61296186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23352576-C-T

http://identifiers.org/hco/2/GRCh38#61296399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23352355-C-A

61296428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23352326-C-G

61296433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23352321-A-G

61296617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23352095-T-C

61296804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 23351572-T-C

61296987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23351390-A-T

61297627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350659-C-T

61297654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23350629-T-C

http://identifiers.org/hco/2/GRCh38#61300806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23344076-A-C

61301281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23343002-A-G

61302242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23341370-G-A

61302303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23341309-A-G

61311106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23339407-A-G

61311106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23339407-A-T

61311321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23339162-T-C

61311520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23338842-A-G

61311763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23338578-A-G

61311763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23338578-A-T

61312014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23338355-T-C

61312759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23337058-T-G

http://identifiers.org/hco/2/GRCh38#61313038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23336671-C-A

61313038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23336671-C-T

61313102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23336594-T-C

http://identifiers.org/hco/2/GRCh38#61313402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23336333-A-C

61314522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23335234-T-G

http://identifiers.org/hco/2/GRCh38#61314865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23334508-A-C

61314865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23334508-A-G

61314992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23334381-G-A

61314992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23334381-G-T

61314993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23334380-G-A

61314993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23334380-G-T

61314998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23334375-T-C

61315123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23334219-T-G

61315286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23334080-T-C

http://identifiers.org/hco/2/GRCh38#61315758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23333915-C-A

61315758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23333915-C-T

61319084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23331456-A-G

61319136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23331416-T-C

61319163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23331387-A-G

61325557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23327310-A-G

61325558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23327309-A-G

http://identifiers.org/hco/2/GRCh38#61325580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23327280-A-C

61325580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23327280-A-G

http://identifiers.org/hco/2/GRCh38#61325721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23326983-A-C

61326691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23326405-T-A

http://identifiers.org/hco/2/GRCh38#61331220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23325141-C-A

http://identifiers.org/hco/2/GRCh38#61331452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23324937-A-C

61331452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23324937-A-G

61333582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23323878-G-T

61333795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23323689-A-G

61333897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: missense variant
orthologous variants: 23323393-G-A

61333897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: missense variant
orthologous variants: 23323393-G-T

61333990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23323291-T-A

61333990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23323291-T-C

61334005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23323277-A-G

61334011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23323271-T-A

61334011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23323271-T-C

61334051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23323228-A-G

61334134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23323071-A-G

61338865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23321060-T-C

61338865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23321060-T-G

61339213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron variant
orthologous variants: 23320704-G-T

61339732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23320202-G-A

61339732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23320202-G-C

61339732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23320202-G-T

61339778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23320154-T-C

61343665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23317666-T-C

61343665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23317666-T-G

61344545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23316473-G-A

61344585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23316434-T-A

61344588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23316431-T-C

61344753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23316256-A-G

61344860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23316150-G-C

61347720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23314660-T-C

61347720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23314660-T-G

61347768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23314612-T-C

61347781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 23314599-T-C

61347917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 23314430-A-T

61348181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: synonymous variant
orthologous variants: 23314166-G-A

61348284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 23313985-T-C

61348284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 23313985-T-G

61348371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 23313898-G-C

61348399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 23313870-T-G

61348953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23312994-T-C

http://identifiers.org/hco/2/GRCh38#61348956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23312991-C-A

61348960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23312987-T-C

61349100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23312777-T-C

61349291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 23312569-G-A

61349386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23312490-G-C

61349386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23312490-G-T

61349516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23312394-A-G

61350235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23311746-C-T

http://identifiers.org/hco/2/GRCh38#61350544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23311426-A-C

61350553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23311417-T-A

61350553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23311417-T-C

http://identifiers.org/hco/2/GRCh38#61350821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23311171-A-C

61350831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23311160-T-A

61350831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23311160-T-C

61350844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23311147-A-T

http://identifiers.org/hco/2/GRCh38#61370222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23305163-C-A

61370280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23305133-G-A

61370565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 23304857-T-C

http://identifiers.org/hco/2/GRCh38#61370918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23304598-C-A

61370918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23304598-C-T

61378353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23301661-T-C

61378405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 23301609-T-A

61378405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 23301609-T-C

61378479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23301542-T-A

61378479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23301542-T-C

61378479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23301542-T-G

http://identifiers.org/hco/2/GRCh38#61378483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23301538-C-A

61378483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23301538-C-T

61378502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23301515-A-G

61379116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23301252-G-A

61380088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23299419-T-C

61380109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23299402-T-C

61380109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23299402-T-G

61380119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23299392-G-C

61380119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23299392-G-T

http://identifiers.org/hco/2/GRCh38#61380433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23298627-A-C

61380442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23298618-T-C

61380442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23298618-T-G

http://identifiers.org/hco/2/GRCh38#61380497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23298553-A-C

61380497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23298553-A-G

61380502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23298548-C-G

61380502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23298548-C-T

61380697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23298374-C-T

61381021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23298069-G-A

61381021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23298069-G-C

61382579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23296315-G-C

61382597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23296295-G-C

61382727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23296175-T-A

61382727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23296175-T-C

61382790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23296123-T-C

61383278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 23295206-T-A

61383278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 23295206-T-C

61383319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 23295165-A-T

http://identifiers.org/hco/2/GRCh38#61383337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23295147-C-A

61383411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23295075-A-G

61394626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23293871-T-C

61394632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23293865-G-A

61394632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23293865-G-C

61394645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23293852-T-G

61394706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23293795-A-T

61394718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23293784-T-C

61394816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23293698-G-A

61395012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23293501-T-C

http://identifiers.org/hco/2/GRCh38#61395045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23293472-A-C

61395359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23293209-A-G

61395366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23293202-A-G

61395457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23293114-T-C

61398936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23290938-T-G

61403474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23286909-T-C

61403519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23286867-T-C

61404425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23285629-C-T

http://identifiers.org/hco/2/GRCh38#61404630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23285440-A-C

61404630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23285440-A-G

61404723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23285368-A-G

61404867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23285231-C-T

61405620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23283951-A-G

61405620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23283951-A-T

61405658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23283910-G-A

61405658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23283910-G-C

61405658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23283910-G-T

61406183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23283375-T-C

61406576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23283021-C-T

http://identifiers.org/hco/2/GRCh38#61407632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23282507-C-A

61407632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23282507-C-G

61407640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23282499-G-A

61408723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23281018-T-A

61408723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23281018-T-C

61420292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23271294-T-G

61420343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23271242-G-A

61420343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23271242-G-T

61420625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23270867-C-G

61420625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23270867-C-T

http://identifiers.org/hco/2/GRCh38#61420654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23270837-C-A

61420654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23270837-C-T

61420719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23270773-G-T

61420816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 23270676-C-T

61420855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23270641-A-T

http://identifiers.org/hco/2/GRCh38#61420856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23270640-A-C

http://identifiers.org/hco/2/GRCh38#61420920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23270573-A-C

61465263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23260293-G-A

61465263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23260293-G-T

61465288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23260269-T-C

61465330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23260226-A-T

61468824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23258676-T-C

http://identifiers.org/hco/2/GRCh38#61469456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23258136-C-A

61469456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23258136-C-T

61470315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23257334-G-C

http://identifiers.org/hco/2/GRCh38#61470378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#23257279-A-C

61470378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 23257279-A-T

http://identifiers.org/hco/2/GRCh38#61470424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23257240-C-A

61470424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23257240-C-G

61470487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 23257181-G-C

61470545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23257121-G-A

61470545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23257121-G-C

61470545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23257121-G-T

61470599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23257066-G-A

61470599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 23257066-G-T

61470774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 5 prime UTR variant
orthologous variants: 23256891-G-A

61470810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 5 prime UTR variant
orthologous variants: 23256855-G-A

61470810-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 5 prime UTR variant
orthologous variants: 23256855-G-C

61470810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 5 prime UTR variant
orthologous variants: 23256855-G-T

61470873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 5 prime UTR variant
orthologous variants: 23256790-T-C

61470873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 5 prime UTR variant
orthologous variants: 23256790-T-G

http://identifiers.org/hco/2/GRCh38#61470916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#23256744-C-A

61470916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20066
most severe consequence: 5 prime UTR variant
orthologous variants: 23256744-C-T