97822035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 59421400-A-G

http://identifiers.org/hco/3/GRCh38#97822091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#59421358-C-A

97822091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 59421358-C-T

97822113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5 prime UTR variant
orthologous variants: 59421336-G-T

97822134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 59421314-T-C

http://identifiers.org/hco/3/GRCh38#97822164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59421292-C-A

97822164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5 prime UTR variant
orthologous variants: 59421292-C-T

http://identifiers.org/hco/3/GRCh38#97822170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59421286-C-A

97822335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 59421126-T-C

97822385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59421088-G-A

97822385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59421088-G-T

97822578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59421011-C-G

97822580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59421010-G-A

97822580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59421010-G-C

97822921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59420859-G-A

97823101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59420650-T-A

97823398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59420351-G-A

97823465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59420286-T-A

97823512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59420242-G-A

97823576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59420177-A-G

97823598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59420155-A-G

97823645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59420113-G-A

97823970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59419842-C-G

97824203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59419585-T-C

http://identifiers.org/hco/3/GRCh38#97824349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59419442-A-C

97824373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59419418-T-A

97824373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59419418-T-C

97824810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59418289-T-C

97825239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59417974-A-G

97825452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59417752-C-T

97825485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59417734-G-A

97825485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59417734-G-C

97825614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59417601-G-C

97825725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59417489-C-T

97826237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59416515-T-G

http://identifiers.org/hco/3/GRCh38#97826481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59416320-C-A

http://identifiers.org/hco/3/GRCh38#97826483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59416318-C-A

97826483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59416318-C-T

97827251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59415440-G-A

97827406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59415288-C-T

97827452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59415242-G-T

97827650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59415057-A-G

97827882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59414845-G-A

97828138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59414601-C-T

97828550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59414243-G-A

97828958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59413862-G-T

97828962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59413858-C-T

97828975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59413845-G-T

97828977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59413843-G-C

97829027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59413795-A-G

97829358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59413503-C-G

http://identifiers.org/hco/3/GRCh38#97829411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59413471-C-A

97829480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59413438-T-C

97829594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59413329-T-C

http://identifiers.org/hco/3/GRCh38#97834198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59410988-A-C

97834250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59410936-G-A

97834250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59410936-G-T

97834386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59410764-T-C

http://identifiers.org/hco/3/GRCh38#97834410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59410740-A-C

97834677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59410517-T-G

97834703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59410487-A-G

http://identifiers.org/hco/3/GRCh38#97834750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59410440-A-C

http://identifiers.org/hco/3/GRCh38#97834833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59410372-C-A

97834858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59410349-T-G

97835046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59410197-A-T

97835119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59410125-G-A

97835235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59410009-G-A

97835383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59409847-G-C

97835386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59409844-C-T

97835488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59409731-T-C

97835488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59409731-T-G

97836180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59408951-C-T

97836188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59408943-C-T

97836213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59408919-C-T

97836368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59408763-T-A

97836558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59408571-A-G

97836616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59408517-G-A

97836616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59408517-G-C

97836714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59408418-G-A

http://identifiers.org/hco/3/GRCh38#97836864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59408286-C-A

97836864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59408286-C-T

http://identifiers.org/hco/3/GRCh38#97837067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59408090-C-A

97837074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59408083-G-T

97837165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407684-G-T

97837220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407645-G-T

97837244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407621-C-T

97837300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407575-G-A

http://identifiers.org/hco/3/GRCh38#97837570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59407307-A-C

97837618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407262-A-T

97837619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407261-G-A

97837668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407199-G-T

97837834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407055-G-A

97837859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59407030-T-C

97838061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59406734-G-A

97838308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59406521-G-A

97838339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59406489-C-T

97838493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59406344-C-G

97838644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59406163-G-A

97838656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59406150-A-G

97838665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59406141-C-T

97838709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59406098-T-A

http://identifiers.org/hco/3/GRCh38#97838767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59406055-A-C

97838767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59406055-A-G

97839147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59405756-T-C

97839179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59405729-T-C

97840004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59403037-A-T

97840890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59401171-T-C

97840937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59401111-A-G

97840947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59401094-G-A

http://identifiers.org/hco/3/GRCh38#97840963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59401078-A-C

97841397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59400040-T-C

97841459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59399980-C-G

http://identifiers.org/hco/3/GRCh38#97841499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59399940-C-A

97841621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59399819-A-G

97841639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59399800-G-C

http://identifiers.org/hco/3/GRCh38#97841712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59399745-C-A

97841712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59399745-C-T

97841748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59399700-T-G

http://identifiers.org/hco/3/GRCh38#97841870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59399579-A-C

http://identifiers.org/hco/3/GRCh38#97842634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59398726-C-A

97842674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59398695-G-C

97842674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59398695-G-T

97842711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59398670-A-G

97842723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59398658-C-T

97843155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59398265-T-C

97843171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59398249-G-A

97843171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59398249-G-T

97843182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59398238-T-C

97843182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59398238-T-G

97843209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59398211-C-T

97843214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59398206-A-G

97843251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59398169-A-G

97843358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59398039-G-A

97843381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59398023-T-A

97843381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59398023-T-C

97843508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59397948-G-A

97843795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59397663-G-A

97843852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59397628-A-G

97843879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59397601-C-T

97843887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59397593-A-G

97843966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59397526-A-G

97844204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59397293-C-G

97844212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59397285-T-G

97844401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396958-T-C

97844481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396883-T-C

97844532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396832-G-A

97844605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396763-T-G

97844616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396752-C-T

97844618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396750-T-C

97844722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396659-G-A

97844762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396616-T-G

97844805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396533-C-T

97845186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395447-C-T

97845322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395315-T-G

97845555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395092-T-C

97845673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394963-C-T

97845822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394833-T-C

97845867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394798-C-T

97845888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394777-A-G

http://identifiers.org/hco/3/GRCh38#97845998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59394695-A-C

97845998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394695-A-G

97846142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394576-A-G

97846268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394460-G-A

97846268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394460-G-C

97846302-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394425-T-G

97846381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394174-C-T

http://identifiers.org/hco/3/GRCh38#97846395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59394160-A-C

97849185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59393083-T-G

97849278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59392997-C-G

97849452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59392929-G-A

97849513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59392874-C-T

http://identifiers.org/hco/3/GRCh38#97849535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59392852-A-C

97849698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59392700-C-T

97849719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59392688-T-C

97849782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59392626-G-A

97852088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391630-G-A

97852139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391559-T-C

97852222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391473-G-T

97852304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391395-A-G

97852449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391269-T-C

97852473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391245-G-A

97859548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59390051-T-G

97859668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389927-A-G

97859668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389927-A-T

http://identifiers.org/hco/3/GRCh38#97859790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59389808-A-C

97859904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389700-A-G

97859960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389678-T-C

http://identifiers.org/hco/3/GRCh38#97859962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59389676-A-C

97860420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389218-G-A

97860631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389053-A-T

97860635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389049-T-C

97860640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389044-C-T

97860657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389026-C-T

97860782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388917-G-T

97861279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388758-T-G

97861288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388749-A-G

http://identifiers.org/hco/3/GRCh38#97861303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59388738-C-A

97861303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388738-C-T

97861315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388725-A-G

97861338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388688-G-A

http://identifiers.org/hco/3/GRCh38#97861376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59388645-A-C

97861956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388097-C-T

97862364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59387904-A-G

97862572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59387726-T-A

97862707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59387594-G-C

97862714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59387583-G-A

97862803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59387501-A-G

97863029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59387252-G-C

97863120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59387161-T-C

97863368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386890-C-T

97863594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386682-T-C

97863594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386682-T-G

97863665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386605-A-G

97863665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386605-A-T

97863666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386604-A-G

97863697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386566-C-T

97863734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386529-G-A

97864093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386114-A-G

97864093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386114-A-T

97864102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386105-G-T

97864192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386022-A-G

97864256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59385965-C-T

97864476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59385745-C-G

97864476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59385745-C-T

97864525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59385696-T-C

97864669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59385536-A-G

97864669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59385536-A-T

http://identifiers.org/hco/3/GRCh38#97864713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59385489-C-A

97865088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59384848-A-G

97865192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59384745-C-T

97868308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383767-G-C

97868447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383652-A-G

97868447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383652-A-T

97868565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383546-A-T

97868672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383451-A-G

97868672-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383451-A-T

97868955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383234-A-G

97869685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382845-C-T

97869701-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382829-T-A

97869726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382814-T-A

97869883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382654-A-T

97869904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382620-T-G

97869918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382606-T-C

97869932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382594-T-G

97869971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382560-A-G

97870002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382528-T-C

97870127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382388-T-C

97870754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381697-G-T

97870767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381684-G-A

http://identifiers.org/hco/3/GRCh38#97870828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59381617-A-C

97870828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381617-A-G

http://identifiers.org/hco/3/GRCh38#97871115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59381325-C-A

97871120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381320-G-A

97871161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381279-T-G

97871182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381260-G-T

97871303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381144-T-C

97871557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380885-C-T

97871590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380842-G-A

97871740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380694-G-A

97871758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380674-G-T

97871943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59380499-C-T

97872001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59380441-T-A

97872002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59380440-G-A

97872130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59380315-C-T

97872138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59380307-A-G

http://identifiers.org/hco/3/GRCh38#97872149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59380296-A-C

97872149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59380296-A-G

97872206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59380239-T-A

97872241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59380204-T-C

http://identifiers.org/hco/3/GRCh38#97872346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59380126-A-C

97872369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59380103-T-A

97872369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59380103-T-C

97872461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59380011-A-G

97872509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59379963-T-C

97872649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59379823-G-C

97872694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59379778-T-A

97872697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59379775-G-A

http://identifiers.org/hco/3/GRCh38#97872756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59379716-A-C

97872818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59379657-T-C

97872818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59379657-T-G

http://identifiers.org/hco/3/GRCh38#97872824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59379651-C-A

97872824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59379651-C-T

http://identifiers.org/hco/3/GRCh38#97872933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59379533-A-C

97872933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59379533-A-G

http://identifiers.org/hco/3/GRCh38#97872996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59379467-C-A

97873106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59379357-G-C

97873127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59379336-C-G

97873127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59379336-C-T

97873151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59379312-A-G

97873194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59379269-G-A

97873257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59379209-T-C

97873331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59379144-G-T

http://identifiers.org/hco/3/GRCh38#97873366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59379112-A-C

97873366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59379112-A-G

97873423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59379055-G-C

97873449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59379029-G-T

97873490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 59378991-G-T

97873595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59378886-G-C

97873595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59378886-G-T

97873711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59378776-C-T

97874031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59378459-C-G

97874073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59378417-G-A

97874090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59378400-G-A

97874090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59378400-G-C

97874146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59378344-A-T

97874153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 59378337-G-T

97874173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59378317-T-A

97874323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59378167-T-C

97874340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59378156-A-G

97874991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59377520-G-A

97875022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59377483-G-T

97875153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59377352-T-G

97875249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59377253-A-G

97875345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59377154-G-T

http://identifiers.org/hco/3/GRCh38#97875409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59377090-A-C

97875409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59377090-A-G

97875453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59377046-A-G

97875485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59377014-A-G

97875498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59377001-G-A

97875498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59377001-G-T

97875503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376996-G-C

97875507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376992-A-G

http://identifiers.org/hco/3/GRCh38#97875519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59376980-C-A

97875586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59376913-T-A

http://identifiers.org/hco/3/GRCh38#97875592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59376907-A-C

http://identifiers.org/hco/3/GRCh38#97875630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59376869-C-A

97875630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376869-C-G

97875641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376861-A-G

97875745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59376757-T-C

97875824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59376678-T-C

97875842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376660-A-G

97875853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59376649-T-C

97875856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59376646-T-C

97875922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376580-G-A

97875929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376573-G-A

97875929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: stop gained
orthologous variants: 59376573-G-T

97875963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376539-A-G

97876005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376497-G-T

97876028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376474-T-G

97876073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376432-A-G

97876153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59376352-G-C

97876153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59376352-G-T

97876158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376347-T-C

97876213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59376292-G-A

97876213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59376292-G-C

97876213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59376292-G-T

97876214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376291-C-T

97876279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59376223-A-G

97876307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376195-G-T

97876411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59376082-A-G

http://identifiers.org/hco/3/GRCh38#97876452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59376038-C-A

97876452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376038-C-G

97876452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376038-C-T

97876457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59376033-G-A

97876465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59376025-C-T

97876523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59375967-A-G

97876523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59375967-A-T

97876591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59375914-T-C

http://identifiers.org/hco/3/GRCh38#97876601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59375904-C-A

97876601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59375904-C-T

97876640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59375862-C-T

97876695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59375804-G-A

97876787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59375712-G-A

97876787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59375712-G-T

http://identifiers.org/hco/3/GRCh38#97876788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59375711-C-A

97876788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59375711-C-T

97876814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: stop gained
orthologous variants: 59375685-G-T

97876827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59375672-A-G

97876829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59375670-T-C

97876843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59375656-A-T

http://identifiers.org/hco/3/GRCh38#97876882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59375614-A-C

97876882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59375614-A-G

http://identifiers.org/hco/3/GRCh38#97876883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59375613-C-A

http://identifiers.org/hco/3/GRCh38#97876955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59375541-C-A

97876955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59375541-C-T

http://identifiers.org/hco/3/GRCh38#97877027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59375469-C-A

97877027-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59375469-C-G

97877039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59375457-A-G

97877147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59375343-A-G

97877564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59374932-T-G

97877654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59374848-G-A

97877665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59374837-A-G

97877761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59374741-C-T

97877770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59374732-T-C

97877822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59374683-G-A

97877842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59374663-G-C

97877845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59374660-C-T

97878008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59374497-A-G

97878044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 59374460-T-A

http://identifiers.org/hco/3/GRCh38#97878089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59374422-C-A

97878089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59374422-C-T

97878106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59374405-T-G

97878239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59374344-T-A

97878239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59374344-T-C

97878469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59374174-T-C

97878469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59374174-T-G

97878477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59374166-A-T

97879076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59373612-T-C

97879327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59373367-C-G

97879372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59373316-G-A

97879463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59373268-G-A

97879518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59373224-G-T

http://identifiers.org/hco/3/GRCh38#97879652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59372981-A-C

97879652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59372981-A-G

97879753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59372886-G-A

97879753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59372886-G-T

97879790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59372844-A-G

97879799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59372835-T-G

97879843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59372781-A-G

97879843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59372781-A-T

97880155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59372479-T-C

97880217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59372421-G-A

97880217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59372421-G-T

97880470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59372181-G-A

http://identifiers.org/hco/3/GRCh38#97880471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59372180-C-A

http://identifiers.org/hco/3/GRCh38#97880626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59372030-C-A

97880675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59371981-A-G

97881059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59370923-T-A

97881131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59370851-A-G

97881237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59370743-T-C

97881241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59370730-A-G

97882575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59369840-A-G

97882599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59369818-A-G

97882683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59369618-T-C

97882940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59369348-A-G

97883305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59369028-G-A

97883305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59369028-G-T

97883329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59369004-A-T

97883365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59368969-A-G

97883595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59368750-G-A

97884108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59367564-A-G

97884130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59367542-A-G

97884281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59368409-G-C

97884417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59368224-G-A

http://identifiers.org/hco/3/GRCh38#97884585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59368068-A-C

http://identifiers.org/hco/3/GRCh38#97884830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59367788-A-C

97885012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59367587-C-T

97885035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59367564-G-A

97886125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59365008-C-T

97886404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59364727-G-A

http://identifiers.org/hco/3/GRCh38#97886561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59364591-C-A

97886645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: synonymous variant
orthologous variants: 59364512-A-G

97886680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59364477-G-A

http://identifiers.org/hco/3/GRCh38#97886713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59364444-A-C

97886713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59364444-A-G

97886742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59364415-G-T

97886746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59364411-C-G

97886746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59364411-C-T

97886792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59364365-T-A

http://identifiers.org/hco/3/GRCh38#97886872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59364266-C-A

97886872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59364266-C-T

97886897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59364238-G-C

97886897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59364238-G-T

97887007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59364127-A-G

97887007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59364127-A-T

97887018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59364116-G-A

97887035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59364103-A-G

97887091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59364051-A-G

97888172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59363804-A-G

97888223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59363759-T-C

97888241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59363741-A-G

97888291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59363702-A-G

http://identifiers.org/hco/3/GRCh38#97888461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59363531-C-A

97888467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59363525-T-A

97888467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59363525-T-C

97888468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59363524-A-G

97888549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59363444-A-G

97888605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59363173-T-G

97888820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59362936-T-C

97888909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59362845-G-T

97888974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59362776-T-C

97889137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59362655-C-T

97889268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59362532-G-A

97889268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59362532-G-T

97889274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59362526-T-C

http://identifiers.org/hco/3/GRCh38#97889302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59362505-C-A

97889302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59362505-C-G

97889525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59362336-G-A

97889525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59362336-G-T

97889662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59362221-A-G

97889776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59362125-A-G

97889831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59362067-T-C

http://identifiers.org/hco/3/GRCh38#97889873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59362014-A-C

97890144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59361764-T-C

97890145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59361763-G-A

http://identifiers.org/hco/3/GRCh38#97890156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59361752-A-C

97890274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59361641-G-C

97890387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59361510-G-A

97890581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59361210-T-C

97890941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59360884-G-A

97890957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59360852-A-G

http://identifiers.org/hco/3/GRCh38#97891060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59360753-C-A

97891061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59360752-A-G

97891287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59360552-C-T

97892809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59360365-A-G

http://identifiers.org/hco/3/GRCh38#97892886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59360273-C-A

97892886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant
orthologous variants: 59360273-C-G

97892953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant
orthologous variants: 59360206-G-T

97892986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, missense_variant
orthologous variants: 59360173-G-C

97893016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59360145-T-C

97893016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59360145-T-G

http://identifiers.org/hco/3/GRCh38#97893043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59360121-C-A

97893043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59360121-C-T

http://identifiers.org/hco/3/GRCh38#97893105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59360060-C-A

97893105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59360060-C-T

97893107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59360058-T-C

97893112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59360053-A-G

97893152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59360006-G-T

http://identifiers.org/hco/3/GRCh38#97893232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59359940-C-A

97893289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59359869-G-A

97893570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59359606-G-C

97893953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59359285-T-C

97894237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59359002-T-C

97894263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59358976-C-G

97894668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59358469-T-C

97895320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59357853-T-C

97895589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59357533-A-G

97895596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59357526-G-A

97895636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59357490-G-A

97895748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59357387-A-G

97895848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59357292-T-C

http://identifiers.org/hco/3/GRCh38#97895854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59357286-C-A

97895920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59357222-T-C

http://identifiers.org/hco/3/GRCh38#97896165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59356983-C-A

97896225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59356941-T-C

97896256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59356910-T-C

97896296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59356692-A-G

97896659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59356313-C-G

97896663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59356309-G-A

97896766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59356214-G-A

97897214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59354554-T-C

97897345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59354412-T-C

97897367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59354389-G-A

97897377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59354379-C-T

97898405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59351288-C-T

97898459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59351234-G-A

97898525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59351173-C-T

97898640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59351056-T-C

http://identifiers.org/hco/3/GRCh38#97898875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59350848-C-A

97898875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 59350848-C-T

http://identifiers.org/hco/3/GRCh38#97899048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59350666-C-A

97899048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59350666-C-G

97899048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59350666-C-T

97899053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59350661-G-A

97899165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59350563-T-C

97899274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59350454-T-C

97900046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59349718-A-G

97900407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59349665-A-G

97900593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59349477-G-T

97900618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59349452-G-T

http://identifiers.org/hco/3/GRCh38#97900764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59349311-C-A

97900764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59349311-C-T

97902719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59348679-T-A

97902872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59348521-T-C

97903161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59348241-C-T

97903196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59348206-T-C

97903418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59347876-A-G

97903608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59347717-T-C

97903825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59347492-G-A

97903871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59347436-G-C

97903884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59347390-T-A

97903892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59347382-G-A

97903892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59347382-G-C

97903892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59347382-G-T

97903956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59347286-G-A

97904444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59346795-A-G

97910934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59346315-A-G

97910939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59346310-C-T

http://identifiers.org/hco/3/GRCh38#97911098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59346144-A-C

97911310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59345931-G-A

97911310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59345931-G-T

97911412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59345800-T-C

97912109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59345385-T-C

97912134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59345360-T-C

97912135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59345359-T-C

http://identifiers.org/hco/3/GRCh38#97912167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59345331-C-A

97912167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 59345331-C-T

http://identifiers.org/hco/3/GRCh38#97912248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59345250-C-A

97912248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59345250-C-T

97912370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59345136-T-C

97912370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59345136-T-G

97913892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59344664-T-C

97913892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59344664-T-G

97913962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59344594-A-G

97914015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59344538-T-A

97914222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59344338-G-A

http://identifiers.org/hco/3/GRCh38#97914236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59344324-A-C

http://identifiers.org/hco/3/GRCh38#97914448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59344104-C-A

http://identifiers.org/hco/3/GRCh38#97914712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59343353-A-C

97914712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59343353-A-G

97914919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59343143-G-A

97914931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59343131-C-G

97915045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59343029-A-G

97915153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59342977-T-A

97915211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59342927-A-G

97915321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59342822-A-T

97915351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59342790-G-A

97915475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59342689-T-G

97915481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59342683-A-G

97915574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59342613-G-A

97915583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59342601-T-C

97915600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59342584-T-C

97915617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59342567-C-T

97915716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense variant
orthologous variants: 59342465-T-C

97915822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59341104-A-G

http://identifiers.org/hco/3/GRCh38#97915829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59341097-C-A

97915829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59341097-C-T

http://identifiers.org/hco/3/GRCh38#97915883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59341041-A-C

97915964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59340980-T-C

97916085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59340847-G-A

97916469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59340537-A-G

97916523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59340483-T-C

97916529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59340477-A-G

97916590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59340418-T-C

97916666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59340342-A-G

97916900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59340094-T-C

97916903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59340091-G-A

97916903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59340091-G-C

97917120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59339880-A-T

97917122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59339878-C-T

97917649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59339871-T-C

97917868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59339661-C-T

97917896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59339638-C-T

97917909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59339625-G-T

97917915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59339622-C-T

97917974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59339566-C-T

97918063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59339503-G-A

97918090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, undefined
orthologous variants: 59339471-A-G

97918185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59339390-G-T

97918313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59339259-A-G

97918494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59339085-T-C

97918586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59338997-T-G

97918619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59338967-A-G

97918783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59338791-A-G

97918804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59338770-G-C

97918984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59338633-T-C

97919033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59338576-A-G

97919100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59338500-G-C

97919248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59338359-A-G

97921101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59336962-T-A

97921101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59336962-T-C

97921101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59336962-T-G

http://identifiers.org/hco/3/GRCh38#97921307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59336223-A-C

97921432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59336102-G-C

97921563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59335980-G-C

97921565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59335978-G-C

97921946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59335627-T-A

97921975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron variant
orthologous variants: 59335599-T-C

97928755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59332229-T-G

97928903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59332075-T-C

97928954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59332024-T-C

97929600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331324-C-G

97929674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331251-C-T

97929675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331250-G-A

97929696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331232-C-T

97929852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59331076-T-G

http://identifiers.org/hco/3/GRCh38#97930122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59330863-A-C

97930523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330330-G-C

97930835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59330044-C-T

97931762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59328566-T-G

97931856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59328482-T-C

97931934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59328406-C-T

97931991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59328336-A-G

97932316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59328044-G-C

97932361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59328000-T-C

97932483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327881-G-A

http://identifiers.org/hco/3/GRCh38#97933659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59326725-A-C

97933662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59326722-C-T

97933814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59326561-G-A

97933814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59326561-G-C

97933814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59326561-G-T

http://identifiers.org/hco/3/GRCh38#97934021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59326277-C-A

97934076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59326215-C-T

97934616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59325699-G-A

97934695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59325613-T-G

http://identifiers.org/hco/3/GRCh38#97934825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59325467-C-A

97935101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59325211-G-A

97936507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59323870-T-C

97936547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59323829-C-T

97936677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59323717-T-C

97936759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59323637-T-A

97936778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59323616-C-T

http://identifiers.org/hco/3/GRCh38#97936789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59323605-A-C

97936951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59323452-G-T

97937042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59323367-G-A

97937042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59323367-G-T

http://identifiers.org/hco/3/GRCh38#97937187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59323223-A-C

97937380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59323003-T-A

97937519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59322868-G-A

97937677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59322694-C-G

97937736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59322631-G-A

97937747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59322620-A-G

97937763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59322607-T-C

97937829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59322556-T-C

97939947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59317197-A-G

http://identifiers.org/hco/3/GRCh38#97940003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59317141-C-A

97940439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316767-C-T

97940550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316672-T-G

97940597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316636-T-G

97940690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316595-T-A

97940752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316532-T-C

97940785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316477-A-G

97940995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316291-A-G

97941005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316281-G-A

97941005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316281-G-C

97941005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316281-G-T

97941007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316279-A-G

97941037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316251-G-A

97941037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316251-G-T

97941066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316222-T-A

97941066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316222-T-C

http://identifiers.org/hco/3/GRCh38#97941073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59316214-C-A

97941099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316188-T-C

97941101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316186-T-C

97941125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59316159-A-G

http://identifiers.org/hco/3/GRCh38#97941139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59316145-C-A

97941380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59315938-T-C

97941449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59315890-T-A

97941581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59315836-C-T

http://identifiers.org/hco/3/GRCh38#97942038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59315423-A-C

http://identifiers.org/hco/3/GRCh38#97942060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59315403-A-C

97942135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59315344-T-C

http://identifiers.org/hco/3/GRCh38#97942187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59315295-C-A

97942288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59315183-G-A

97942359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59315112-G-T

97942425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59315046-C-T

97942467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59315004-G-A

97942498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314977-A-T

97942642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314710-T-C

97942642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314710-T-G

http://identifiers.org/hco/3/GRCh38#97942647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59314705-C-A

97942647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314705-C-T

97942686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314498-T-C

http://identifiers.org/hco/3/GRCh38#97942692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59314489-C-A

97942692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314489-C-G

97942692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314489-C-T

97942773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314421-T-A

97942773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314421-T-C

97942819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314375-C-T

97942887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314315-G-T

97942918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314281-A-T

97942930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314271-T-C

97942949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314248-T-C

97942985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314225-G-C

97942985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314225-G-T

97942999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59314211-C-T

97943273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59313999-G-A

97943425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59313877-T-C

97943457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59313844-G-A

97943457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59313844-G-T

97943475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59313831-T-A

97943475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59313831-T-C

http://identifiers.org/hco/3/GRCh38#97943554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59313768-C-A

97943554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 59313768-C-G

97943608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59313717-T-C

http://identifiers.org/hco/3/GRCh38#97943609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59313716-C-A

http://identifiers.org/hco/3/GRCh38#97943612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59313713-C-A

97943612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59313713-C-T

http://identifiers.org/hco/3/GRCh38#97943616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59313709-A-C

97943616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59313709-A-G

http://identifiers.org/hco/3/GRCh38#97943621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59313704-A-C

97943626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59313699-T-C

97943629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59313696-T-C

97943636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59313689-G-T

97943642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59313680-T-C

97943665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59313659-T-C

97943699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59313633-G-T

97943711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59313623-A-G

http://identifiers.org/hco/3/GRCh38#97943898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59313412-C-A

http://identifiers.org/hco/3/GRCh38#97943901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59313409-A-C

97943938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59313366-T-C

97943998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59313304-A-T

http://identifiers.org/hco/3/GRCh38#97944333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59313074-C-A

97944333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59313074-C-G

97944399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59313016-T-C

97944637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59312777-G-A

97944656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59312758-G-T

97944737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59312693-G-T

http://identifiers.org/hco/3/GRCh38#97944797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 34427
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#59312633-A-C