63998702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7175261-G-A

63998702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7175261-G-C

63998702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7175261-G-T

http://identifiers.org/hco/11/GRCh38#63998804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7175135-C-A

63998804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7175135-C-T

63998928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7175013-G-A

63998972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7174959-G-A

63999061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7174867-G-A

63999061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7174867-G-T

63999080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7174851-G-A

63999080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7174851-G-T

http://identifiers.org/hco/11/GRCh38#63999357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/19/GRCm39#7174561-C-A

63999357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7174561-C-G

63999357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7174561-C-T

http://identifiers.org/hco/11/GRCh38#63999444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7174480-C-A

63999444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174480-C-T

63999449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174474-C-G

63999449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174474-C-T

http://identifiers.org/hco/11/GRCh38#63999457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7174466-C-A

63999460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174463-T-G

63999464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174459-C-G

63999464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174459-C-T

http://identifiers.org/hco/11/GRCh38#63999480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7174443-C-A

63999480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174443-C-G

63999480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174443-C-T

63999585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174343-G-A

http://identifiers.org/hco/11/GRCh38#63999618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7174297-C-A

63999618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174297-C-T

63999715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7174200-C-T

63999733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7174182-T-A

63999733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7174182-T-C

63999766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 7174149-A-G

63999771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 7174143-G-A

63999771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 7174143-G-T

63999783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174131-C-G

63999783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174131-C-T

http://identifiers.org/hco/11/GRCh38#63999961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7174063-C-A

63999961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174063-C-T

63999979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174045-G-A

63999979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174045-G-C

63999979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174045-G-T

http://identifiers.org/hco/11/GRCh38#64000022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7174022-C-A

64000022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174022-C-G

64000022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7174022-C-T

http://identifiers.org/hco/11/GRCh38#64000057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7173987-C-A

64000057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7173987-C-T

64000230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7173890-T-G

64000253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7173867-G-A

64000253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7173867-G-T

http://identifiers.org/hco/11/GRCh38#64000325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7173795-C-A

64000325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7173795-C-G

64000325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7173795-C-T

64000401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7173710-G-A

64000401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7173710-G-T

http://identifiers.org/hco/11/GRCh38#64000408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7173705-C-A

64000408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7173705-C-T

http://identifiers.org/hco/11/GRCh38#64000422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7173691-C-A

64000422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7173691-C-T

http://identifiers.org/hco/11/GRCh38#64000491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7173634-C-A

http://identifiers.org/hco/11/GRCh38#64000983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7173307-C-A

64000983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7173307-C-T

http://identifiers.org/hco/11/GRCh38#64000992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7173298-C-A

64000992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7173298-C-T

64001016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7173274-G-A

64001016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7173274-G-C

64001016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7173274-G-T

64001039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7173246-G-A

64001039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7173246-G-T

64001073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7173218-G-A

64001073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7173218-G-T

http://identifiers.org/hco/11/GRCh38#64001335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7173005-C-A

64001335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7173005-C-T

http://identifiers.org/hco/11/GRCh38#64001527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7172830-C-A

64002371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7171417-G-T

64002636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7171199-G-A

64002636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7171199-G-T

http://identifiers.org/hco/11/GRCh38#64002646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7171189-C-A

64003716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7170812-G-C

http://identifiers.org/hco/11/GRCh38#64003724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7170804-A-C

64003786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7170712-A-G

64003816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7170675-T-C

64004188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7170303-G-A

64004197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7170294-G-A

64004197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7170294-G-T

64004611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7169960-T-C

64004623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7169947-C-T

64004624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7169946-C-T

64004649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7169922-G-A

64004649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7169922-G-T

64005851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7169320-G-A

64005934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7169243-G-A

64006172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7169022-A-G

64006224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7168996-C-T

64007022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7168307-T-A

64007022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7168307-T-C

64007043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7168286-C-T

64007352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7168097-C-T

64008120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7167067-C-T

64008213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7166982-C-G

64008213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7166982-C-T

64008546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7166620-G-A

64008546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7166620-G-C

64008589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7166590-C-T

http://identifiers.org/hco/11/GRCh38#64008874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7166322-C-A

64008898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7166298-G-A

64009099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7166099-T-C

64009153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7166045-A-T

http://identifiers.org/hco/11/GRCh38#64009188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7166016-C-A

64009188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7166016-C-T

64009263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7165942-G-A

64009263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7165942-G-T

64009280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7165925-G-T

64009287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7165918-G-T

64009495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7165733-G-C

64013384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7164723-G-A

64013492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7164583-G-A

64013968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7164012-C-G

64014509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7163570-G-A

64015087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7163112-C-G

64015327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7162879-G-A

64015327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7162879-G-T

64015328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7162878-G-A

64015328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7162878-G-T

64015330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7162876-G-A

64015330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7162876-G-T

64015337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7162869-T-A

64015337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7162869-T-C

64015412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7162800-T-C

64015451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7162765-G-A

64015473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7162744-G-A

64015754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7161856-G-A

64015840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7161740-C-T

64015865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7161714-G-A

64016115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7161487-C-G

64016161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7161442-C-T

64016162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7161441-G-A

64016162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7161441-G-T

64016278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7161317-C-T

64016331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7161262-G-A

64016331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7161262-G-T

64016415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7161203-T-C

64016555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7161097-G-A

64016557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7161095-G-A

http://identifiers.org/hco/11/GRCh38#64017615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7160069-C-A

http://identifiers.org/hco/11/GRCh38#64017776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7159904-C-A

64017776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7159904-C-T

64018034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7159652-G-A

64018038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7159648-A-T

64019398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7158447-C-T

64020743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7157150-T-A

64020960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156958-A-G

64020966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156952-C-T

64021141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156870-G-A

64021607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156422-G-A

64021653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156375-T-G

64021657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156371-G-T

http://identifiers.org/hco/11/GRCh38#64021975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7156120-A-C

64021975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156120-A-G

64021975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156120-A-T

64022083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156029-G-A

64022130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7156004-C-T

64022199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7155952-C-T

64022347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7155821-C-T

64022464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7155725-C-T

64022488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7155701-G-A

64022511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7155689-C-T

64022669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7155532-G-T

64022717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7155483-C-T

64022812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7155393-G-A

64023761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7154372-A-G

64023860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7154283-C-T

64024423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7153807-G-C

64024539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7153697-C-T

64024594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7153645-C-G

64024594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7153645-C-T

64026354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7152178-G-A

64026423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7152116-C-T

http://identifiers.org/hco/11/GRCh38#64026424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7152115-A-C

64026504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7152057-G-A

http://identifiers.org/hco/11/GRCh38#64026763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7151815-C-A

64026763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7151815-C-T

64027224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7151235-C-T

64027710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7150798-T-C

64027740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7150768-C-T

64027886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7150649-T-C

64028279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7150127-T-C

64028438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7149977-G-A

64028535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7149920-G-A

64028784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7149688-C-G

64028847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7149641-C-T

64028873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7149614-G-C

64029430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7149129-G-A

64029489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7149071-T-G

64029650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7148942-C-T

64029982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7148706-G-A

64029982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7148706-G-T

64030178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7148571-C-T

64031172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146820-G-A

64031392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146610-C-G

64032251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146263-T-C

64032273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146251-T-C

64032404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146134-T-C

64032408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7146129-T-C

64032747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7145810-A-G

64032755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7145802-G-A

64032979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7145576-G-A

64033300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7145281-C-T

http://identifiers.org/hco/11/GRCh38#64033307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7145274-C-A

64033310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7145271-T-C

64033992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7145169-T-G

64034240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7144937-G-A

64034643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7144563-G-A

64035297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7143908-C-T

64035448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7143782-C-T

64035622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7143584-G-A

http://identifiers.org/hco/11/GRCh38#64036207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7143022-C-A

64036368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7142880-G-A

64036368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7142880-G-T

64036411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7142836-G-A

64036434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7142813-A-G

http://identifiers.org/hco/11/GRCh38#64036471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7142776-C-A

64036544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7142701-G-C

64036612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7142624-C-T

64037252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7141983-A-T

64037352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7141861-C-T

64037582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7141623-T-C

64037593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7141613-G-A

64037993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7141148-C-T

64038007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7141134-G-T

64038081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7141083-G-A

64038305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7140856-G-A

64038306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7140855-G-A

64039089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7139811-C-T

64039112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7139789-T-C

64039203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7139711-G-A

64039621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7139409-C-G

64039738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7139282-C-T

64039897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7139108-G-A

64040174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7138893-C-T

64040596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7138410-G-A

64040596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7138410-G-C

http://identifiers.org/hco/11/GRCh38#64041085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7138036-C-A

http://identifiers.org/hco/11/GRCh38#64041135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7137977-C-A

64041378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7137744-C-T

64041480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7137648-G-A

64041480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7137648-G-C

64042033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7137180-C-G

64042225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7137028-T-A

64042279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7136970-C-T

64042496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7136858-G-T

64042567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7136843-C-T

64042724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7136807-C-G

http://identifiers.org/hco/11/GRCh38#64043733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7135943-A-C

64044865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7135588-G-A

64044915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7135549-G-A

64045222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7135309-G-A

64045223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7135308-T-G

64045858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7134748-A-G

64046151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7134602-T-A

64046181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7134572-G-A

64046205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7134570-G-T

64046240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7134538-G-A

64047081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7133846-C-T

64048666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7132328-C-G

64049773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7131798-C-T

64049784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7131786-G-C

64050382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7131309-A-G

64050417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7131243-C-T

64051930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7130434-T-G

64052046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7130346-G-C

64052046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7130346-G-T

64052793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7129640-A-G

64052832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7129607-G-A

64053145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7129301-G-A

64053511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7128926-T-C

64053533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7128904-A-T

64053829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7128629-G-A

http://identifiers.org/hco/11/GRCh38#64053848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#7128610-A-C

64053848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7128610-A-G

64053974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7128020-C-T

64053982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7128014-G-A

64053995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7128001-T-C

64054123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7127863-C-G

64054126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7127860-G-A

64054391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7127553-C-G

64054545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7127395-G-A

64054586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7127370-T-C

64054875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7127089-G-A

64055607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7126467-C-T

64056450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7125742-A-G

64056519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7125674-G-A

64056545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7125650-G-A

http://identifiers.org/hco/11/GRCh38#64056558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7125624-A-C

64056728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7125524-G-T

64056731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7125521-G-A

64056821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7125460-C-T

64057251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7125068-A-T

64057540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7124806-G-A

http://identifiers.org/hco/11/GRCh38#64057629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7124733-C-A

http://identifiers.org/hco/11/GRCh38#64057833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7124542-C-A

64057906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7124468-G-A

64057910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7124464-C-G

64057910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7124464-C-T

http://identifiers.org/hco/11/GRCh38#64058687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7123855-A-C

64058753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7123788-T-C

64059087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7123451-C-T

64059115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7123426-G-A

64059276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7123307-C-T

64059417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7123164-T-C

64059814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7122627-G-C

64059814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7122627-G-T

64059819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7122622-G-A

64059861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7122582-G-A

64060023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7122439-C-T

64060424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7122041-A-G

64060680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7121667-T-C

64060688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7121659-T-C

64060692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7121655-T-C

64060969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7121413-G-A

64061008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7121381-C-G

64061008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7121381-C-T

64061410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120890-C-T

64061510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120716-C-G

64061510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120716-C-T

64061600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120620-G-T

64061723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120510-A-T

64061745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120489-G-T

64061969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7120168-C-T

64062156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7119967-G-A

64062177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7119946-C-T

64062203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7119935-A-G

http://identifiers.org/hco/11/GRCh38#64062591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7119621-C-A

64062611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7119601-G-A

64062683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7119534-A-G

64062995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7119370-C-T

64062999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7119366-C-T

64063192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7119245-G-T

64063349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7119127-G-A

64063557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7118989-G-C

64063857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7118728-C-T

64064816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7117838-G-T

64066492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7117170-G-A

64066604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7117087-T-A

64066951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7116788-C-T

64067374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7116431-A-T

64067457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7116348-C-T

64067507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7116302-A-G

64067808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7115990-C-T

64068136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7115658-G-A

64068401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7115435-G-A

64068497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7115342-T-C

64068525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7115319-C-T

64068565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7115278-C-T

64069171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114796-G-A

64069179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114788-A-G

64069216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114765-C-T

64069265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114716-C-T

64069312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114667-G-A

64069761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114304-G-A

64069761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114304-G-T

64069823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114257-C-T

64069931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114153-C-T

64070060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7114044-C-G

64070386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7113732-C-T

64070564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7113552-G-A

64070851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7113282-G-A

64070892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7113245-T-C

http://identifiers.org/hco/11/GRCh38#64071186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7112978-C-A

64071204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7112966-C-T

64071375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7112809-C-T

http://identifiers.org/hco/11/GRCh38#64071593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7112618-A-C

http://identifiers.org/hco/11/GRCh38#64071671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7112553-C-A

64071776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7112465-C-T

64072258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7112059-G-C

64072258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7112059-G-T

64072414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7111960-C-T

64072486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7111889-A-G

http://identifiers.org/hco/11/GRCh38#64072489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7111886-A-C

64072774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7111693-T-A

64073269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7111322-C-G

64073701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7110892-C-G

64073843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7110722-C-T

64074813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7109856-G-C

http://identifiers.org/hco/11/GRCh38#64075330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7109366-A-C

64075332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7109355-T-G

http://identifiers.org/hco/11/GRCh38#64075364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7109313-A-C

64075431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7109259-C-T

64075529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7109165-C-T

64075666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7109036-T-C

64075737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7108930-A-G

64075801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7108872-T-C

64075864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7108803-G-A

64076787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7107980-A-G

64076916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7107861-C-T

64076977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7107815-G-A

64077298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7107537-A-T

64077916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106968-G-A

64077987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106915-C-T

64078322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106750-T-C

64078615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106486-G-A

64078615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106486-G-C

64078926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7106217-T-C

64079187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105978-G-A

64079268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105947-C-G

64079691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105719-G-A

64079692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105718-G-A

64079810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105636-G-A

http://identifiers.org/hco/11/GRCh38#64080075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7105373-C-A

64080075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105373-C-T

64080160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7105294-G-C

64080579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7104022-G-C

64080757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7103798-G-A

64080757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7103798-G-T

64081104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7103511-C-G

64081352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7103338-G-A

64081400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7103292-G-A

http://identifiers.org/hco/11/GRCh38#64081830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7102916-C-A

64082009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7102771-G-T

64082019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7102758-C-T

64082024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7102753-C-T

64082163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7102667-A-G

http://identifiers.org/hco/11/GRCh38#64082172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7102660-C-A

64082172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7102660-C-T

64082182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7102650-C-T

64082224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7102627-G-A

64082224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7102627-G-C

64082323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7102549-G-A

64083466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7100731-A-G

http://identifiers.org/hco/11/GRCh38#64084225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7099836-A-C

64084326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099734-T-C

http://identifiers.org/hco/11/GRCh38#64084425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7099689-C-A

64084425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099689-C-T

http://identifiers.org/hco/11/GRCh38#64084811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7099481-C-A

64084811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099481-C-T

64084874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099427-G-T

64084880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099413-T-C

64085109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099260-A-G

64085160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099207-T-C

64085160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099207-T-G

64085597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7098798-G-A

64085677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7098724-C-G

64085677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7098724-C-T

64086006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7098316-A-G

64086006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7098316-A-T

64086033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7098277-C-T

64086570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7097872-G-T

64086576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7097866-G-A

http://identifiers.org/hco/11/GRCh38#64086590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7097851-C-A

64086590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7097851-C-T

http://identifiers.org/hco/11/GRCh38#64086620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7097818-C-A

64086786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7097671-G-T

http://identifiers.org/hco/11/GRCh38#64086828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7097637-C-A

64086846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7097633-T-G

64086894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7097592-G-A

64086894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7097592-G-T

http://identifiers.org/hco/11/GRCh38#64086917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7097571-C-A

64086917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7097571-C-T

http://identifiers.org/hco/11/GRCh38#64087003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#7097426-C-A

64087003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7097426-C-T

64087023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7097406-T-A

64087023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7097406-T-C

64087024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7097405-G-T

http://identifiers.org/hco/11/GRCh38#64087051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7097368-C-A

64087092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7097328-T-C

http://identifiers.org/hco/11/GRCh38#64087214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7097209-C-A

64087214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7097209-C-T

64087262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7097123-A-G

http://identifiers.org/hco/11/GRCh38#64087286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7097112-C-A

64087286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7097112-C-T

http://identifiers.org/hco/11/GRCh38#64087292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7097106-C-A

64087292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7097106-C-T

64087304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7097094-G-A

64087304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7097094-G-T

64087311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7097092-G-A

http://identifiers.org/hco/11/GRCh38#64087342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7097062-A-C

64087476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096889-C-T

64087478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096887-A-G

64087534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096825-C-T

64087730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096598-T-C

64090127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094660-T-G

64090915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7093896-A-G

64091326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7093736-C-T

64091447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7093632-G-A

64091457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7093621-A-G

64092048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7093113-A-G

64092227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7092931-G-A

64092605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7092556-C-G

64092855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7092378-G-A

64092909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7092328-C-T

64093705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7092098-G-A

64093779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7091997-T-G

64093935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7091860-C-T

64094942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7091235-C-T

64094944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7091233-C-T

http://identifiers.org/hco/11/GRCh38#64094989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7091194-C-A

64094989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7091194-C-T

64095036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7091148-C-T

64096281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089554-C-T

64096300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089535-C-T

64096336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089502-C-T

64096349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089490-G-T

http://identifiers.org/hco/11/GRCh38#64096933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7089184-C-A

64096933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089184-C-G

64097013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089120-G-C

http://identifiers.org/hco/11/GRCh38#64097020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7089113-C-A

64097023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089110-G-C

64097188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088972-A-G

64097642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088519-G-T

64097689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088474-C-T

64098764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7087483-C-T

64098905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7087347-C-T

64099276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7087065-G-T

64099758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086781-A-G

64099908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7086662-G-C

64100414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7086254-T-G

64100670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7085945-C-T

64100894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7085754-G-T

64101367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7085053-C-T

64101519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7084915-C-G

64101519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7084915-C-T

http://identifiers.org/hco/11/GRCh38#64101877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7084611-A-C

64102004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7084510-C-T

64102596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7083999-G-A

64102657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7083835-G-C

64103102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7083462-A-G

64103111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7083449-T-C

64103144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7083411-G-A

64103144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7083411-G-T

64103158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7083399-G-A

64103208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7083351-A-G

64103263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7083299-G-A

64103263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7083299-G-T

64103361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7083201-G-T

http://identifiers.org/hco/11/GRCh38#64103393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7083171-C-A

64103393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7083171-C-T

64103457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7083091-T-C

64103620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7082904-G-A

64103620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7082904-G-T

http://identifiers.org/hco/11/GRCh38#64103632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7082892-C-A

http://identifiers.org/hco/11/GRCh38#64103674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7082852-C-A

64103755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7082767-C-T

64103829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7082732-C-T

http://identifiers.org/hco/11/GRCh38#64103947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7082620-C-A

64103947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7082620-C-T

64103949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7082618-G-A

64103949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7082618-G-T

64103985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7082590-C-G

http://identifiers.org/hco/11/GRCh38#64103986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7082589-C-A

64103986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7082589-C-T

64103992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7082583-T-C

64104123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7082505-C-G

64104158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7082472-T-C

64104202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7082428-A-G

http://identifiers.org/hco/11/GRCh38#64104275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7082331-C-A

64104701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7082013-A-G

64105070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7081673-C-T

64105228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7081529-C-G

64105364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7081376-G-A

64105427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7081309-T-C

64105652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7081162-C-T

64105654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7081160-C-T

64105969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7080975-T-G

64105970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7080974-G-T

64105980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7080964-C-G

64105980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7080964-C-T

http://identifiers.org/hco/11/GRCh38#64106289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7080765-A-C

64106364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7080690-A-G

64107091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7080087-C-T

64107351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7079842-T-A

64107351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7079842-T-C

http://identifiers.org/hco/11/GRCh38#64107498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7079701-C-A

64107498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7079701-C-T

64110173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7078159-G-A

64110185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7078147-C-T

64110207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7078126-T-A

64110245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7078068-T-A

64110245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7078068-T-C

http://identifiers.org/hco/11/GRCh38#64110281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7078029-C-A

64110282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7078028-T-C

64111423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7077037-A-G

64111450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7077005-C-T

64111584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7076889-G-A

64111834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7076697-G-A

64112008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7076564-C-T

64112231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7076364-A-T

64114744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7075887-C-G

http://identifiers.org/hco/11/GRCh38#64114749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7075882-C-A

64115123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7075503-C-T

64115382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7075208-T-C

64115673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7074962-C-G

64115673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7074962-C-T

64115770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7074886-C-T

64116031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7074750-C-T

64116032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7074749-G-A

http://identifiers.org/hco/11/GRCh38#64116096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7074674-C-A

64116096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7074674-C-T

http://identifiers.org/hco/11/GRCh38#64116097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7074673-C-A

64116097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7074673-C-T

64116098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7074672-G-A

64116098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7074672-G-T

64116559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7074252-A-G

64116622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7074189-G-C

64116653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7074158-T-G

64116704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7074107-C-T

64116787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7074024-G-A

64116790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7074021-G-A

64116790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7074021-G-T

64116880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7073931-C-G

64117001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7073810-G-A

64117001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7073810-G-T

64117296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 7073515-G-A

64117396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7073415-G-A

64117504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7073307-A-G

64117864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7072947-T-C

64118257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 7072554-G-A

64118299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7072513-C-T

http://identifiers.org/hco/11/GRCh38#64118304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7072508-C-A

64118304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7072508-C-T

64118422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7072409-G-T

64118453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7072378-G-T

64118508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7072322-A-T

64118574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7072267-T-C

64118574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7072267-T-G

http://identifiers.org/hco/11/GRCh38#64118585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7072256-C-A

64118585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7072256-C-G

64118585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7072256-C-T

64118714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7072111-G-A

64118980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7071845-T-C

64118991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7071834-C-T

64119039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7071781-G-A

64119039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7071781-G-T

64119052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7071768-T-G

64119092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7071729-G-A

64119092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7071729-G-C

64119092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7071729-G-T

64119204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7071617-A-G

http://identifiers.org/hco/11/GRCh38#64119206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7071615-C-A

64119206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7071615-C-T

http://identifiers.org/hco/11/GRCh38#64119735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7071146-C-A

64119994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070889-A-T

64120036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070847-T-C

64120037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070846-G-A

64120098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070785-G-A

64120098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070785-G-C

64120276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070571-C-T

64120282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7070565-C-T

64121525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069818-C-T

64122032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069306-C-T

64122303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069049-G-C

64122326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7069035-C-G

64122461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7068914-C-T

64122623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7068785-A-G

64122673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7068759-G-T

64122778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7068673-C-T

64122849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7068579-C-G

64123656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7067780-G-A

64124368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7067246-T-A

64124459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7067150-G-A

64124540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7067073-T-C

64124543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7067070-C-T

http://identifiers.org/hco/11/GRCh38#64124973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7066787-C-A

64125006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066755-C-T

64125194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066581-C-T

64125544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7066397-G-A

64126036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065925-A-G

64126489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065513-G-A

64126784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065286-G-T

64126909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7065217-G-A

64126909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7065217-G-T

64126983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065138-G-A

64126983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065138-G-T

64127073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065045-G-A

64127073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065045-G-C

64127073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7065045-G-T

64127691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7064333-A-G

64127881-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7064132-A-T

64128051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7063971-C-T

64128086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7063917-G-A

64128261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7063754-C-T

64128274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7063740-C-T

64128374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7063639-T-C

64128596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7063421-G-A

64130678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7062523-C-T

64130915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7062292-C-T

64131720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7061528-G-A

http://identifiers.org/hco/11/GRCh38#64132593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7060699-C-A

64133236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7059752-C-G

64133818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7059248-G-A

64133940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7059146-G-A

64133940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7059146-G-T

64134330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7058228-C-T

64134417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7058145-G-C

http://identifiers.org/hco/11/GRCh38#64134646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7057974-C-A

64134646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7057974-C-T

64134869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7057751-G-C

64135058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7057401-C-T

64135167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7057304-G-A

64135574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7056988-A-G

64135625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7056936-A-G

http://identifiers.org/hco/11/GRCh38#64135677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7056885-C-A

64135809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7056764-C-G

64135875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7056713-C-T

64135990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7056637-G-C

64136007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7056618-C-T

64136357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7056390-G-A

64136435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7056341-T-C

64136540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7056234-G-A

64136621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7055633-T-C

64137007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7055290-G-C

64137007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7055290-G-T

64137954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7052322-A-T

64137992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7052284-G-A

64138099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7052165-G-A

64138122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7052143-G-A

64138399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7051809-G-A

http://identifiers.org/hco/11/GRCh38#64138584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7051620-C-A

64138610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7051595-G-T

64138698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7051516-G-T

64139449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7050714-C-T

64141373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7050006-G-C

64141743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7049700-G-A

64141793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7049676-T-C

64142145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7049351-C-T

http://identifiers.org/hco/11/GRCh38#64142320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7049278-A-C

64142456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7049214-G-C

64142572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7049119-C-G

64144691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7048111-G-T

64144735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7048025-G-A

64144769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7047988-A-G

64145092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7047627-G-A

64145099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7047620-G-A

64145112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7047606-G-A

64145138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7047580-C-T

64145210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7047513-T-C

64145211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7047512-G-A

64145211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7047512-G-T

64145408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7047302-C-T

64145614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7047121-G-A

64145914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7046934-C-G

64145914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7046934-C-T

64145968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7046918-C-G

64148108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7046304-G-T

64148115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7046296-G-A

64148523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7045966-T-C

64148798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7045694-T-C

64148798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7045694-T-G

64148804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7045688-C-T

http://identifiers.org/hco/11/GRCh38#64148819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#7045673-C-A

64148819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7045673-C-T

64148836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7045620-G-A

64148836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 7045620-G-T

http://identifiers.org/hco/11/GRCh38#64148891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7045569-A-C

64148952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7045538-G-A

64148952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7045538-G-T

64149096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7045445-G-C

64149105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7045437-G-A

64149105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7045437-G-T

64149130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7045412-C-T

64149365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7045228-G-A

64149480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7045161-G-A

64149480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7045161-G-C

64149534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7045099-C-T

64149542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7045090-T-C

http://identifiers.org/hco/11/GRCh38#64149671-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7045013-A-C

64149685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7044998-G-A

64150341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7044444-G-A

http://identifiers.org/hco/11/GRCh38#64150461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7044327-A-C

64150463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7044325-A-G

64150644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7044148-A-G

64150702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7044110-G-A

64151055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7043746-G-A

64151098-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7043703-T-A

64151098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7043703-T-C

64151130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7043671-A-G

64151155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7043645-G-T

64151205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7043603-G-A

64151205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7043603-G-T

64151225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7043583-G-T

64151284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7043524-G-A

64151420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7043401-G-A

64151420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7043401-G-T

http://identifiers.org/hco/11/GRCh38#64152192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7043026-C-A

64152192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7043026-C-T

64152201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7043017-T-C

64152246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042973-C-G

64152246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042973-C-T

64152256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042963-G-T

64152354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7042870-T-C

64152471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042775-G-A

64152471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042775-G-C

64152471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042775-G-T

64152498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042748-T-C

64152929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042382-A-G

64152940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042372-G-A

64152940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042372-G-C

64152967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7042347-C-T

64153032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7042294-C-T

64153159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7042193-G-A

http://identifiers.org/hco/11/GRCh38#64156000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7040806-C-A

64156000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7040806-C-T

64156823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7040093-T-C

http://identifiers.org/hco/11/GRCh38#64157125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7039989-C-A

64157385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7039599-C-T

64157697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7039301-A-T

http://identifiers.org/hco/11/GRCh38#64158012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7039028-C-A

64158027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7039014-G-A

64158107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7038934-T-C

64158187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7038865-G-A

64158200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7038852-C-T

64158690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7038613-A-G

64158698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7038605-G-A

64164256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035704-G-A

64164263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035697-C-T

64164339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035610-G-A

64164639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035354-G-A

64164639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035354-G-C

64164799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7035234-G-A

64165096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7034927-G-A

64165601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034605-G-A

64165601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7034605-G-T

http://identifiers.org/hco/11/GRCh38#64165726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#7034519-C-A

64165726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7034519-C-T

64165839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7034412-G-A

64165839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7034412-G-C

64165839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7034412-G-T

64165843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7034408-A-G

64166060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 7034185-T-C

http://identifiers.org/hco/11/GRCh38#64166097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#7034147-C-A

64166097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29598
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 7034147-C-T