29268353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5049003-A-G

http://identifiers.org/hco/22/GRCh38#29268397-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#5048959-A-C

29268592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5048751-G-C

29268685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5048661-C-T

29268759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5048566-C-T

29268874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5048438-C-T

29268915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5048409-A-G

29269146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5048230-G-T

29269149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5048227-G-T

29269174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5048202-G-A

29269266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5048133-G-A

29269266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5048133-G-T

http://identifiers.org/hco/22/GRCh38#29269491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5047928-C-A

29269491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5047928-C-T

http://identifiers.org/hco/22/GRCh38#29269501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5047918-C-A

29269501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5047918-C-T

29270015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5047453-G-T

29270099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5047285-A-G

29271012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5046211-A-G

29271396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5045365-T-G

29271474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5045284-T-G

29271479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5045279-A-G

29271507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5045249-G-A

29271514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5045242-C-G

29272003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5044101-T-G

http://identifiers.org/hco/22/GRCh38#29272149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5043955-C-A

29272149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5043955-C-T

http://identifiers.org/hco/22/GRCh38#29272198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5043916-C-A

29272198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5043916-C-T

29272308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5043812-G-A

29272308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5043812-G-C

29272466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5043644-C-G

29272466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5043644-C-T

29272468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5043643-A-T

29272547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5043505-A-G

http://identifiers.org/hco/22/GRCh38#29272554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5043498-C-A

29272554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5043498-C-T

29272572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5043458-T-A

29273373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5042271-G-A

29273516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5042199-A-G

29273607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5042124-G-A

29273607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5042124-G-C

29273607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5042124-G-T

29273692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5042026-T-C

http://identifiers.org/hco/22/GRCh38#29273936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5041788-C-A

29273936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5041788-C-T

29273947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5041777-A-G

http://identifiers.org/hco/22/GRCh38#29274008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5041721-C-A

29274008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5041721-C-G

29274008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5041721-C-T

29274097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5041630-T-C

29274542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5041214-T-C

http://identifiers.org/hco/22/GRCh38#29274758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5040991-C-A

29274836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5040937-T-G

29274867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5040914-T-C

29275066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5040791-A-T

29275407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5040449-A-G

29275536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5040321-G-A

29275551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5040306-A-T

29275709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5040185-A-G

29275756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5040153-G-A

29275987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5039970-G-A

29275987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5039970-G-T

29275995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5039962-G-T

http://identifiers.org/hco/22/GRCh38#29276070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5039891-C-A

29276188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5039776-G-A

29276188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5039776-G-T

29276261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5039669-T-C

29276416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5039535-G-T

29276610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5039107-T-C

29277750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5038386-G-A

29277750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5038386-G-C

29277752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5038384-G-A

29277923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5038248-A-G

http://identifiers.org/hco/22/GRCh38#29277928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5038243-C-A

29277939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5038232-A-G

29277957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5038213-T-C

29278034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 5038140-T-A

29278056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5038118-G-C

29278077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5038097-G-A

29278077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5038097-G-C

29278170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5038004-G-A

http://identifiers.org/hco/22/GRCh38#29278281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5037888-C-A

29278281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5037888-C-T

29279046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5037757-G-A

29279149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5037664-T-G

29279308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5037523-G-A

29279933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5036851-T-C

29280551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5036576-G-C

29280631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5036506-T-G

29282247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5036213-T-G

29282292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5036180-G-A

http://identifiers.org/hco/22/GRCh38#29282380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5036071-C-A

29282380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5036071-C-T

29282767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035790-T-C

29282773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035784-T-C

29282774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035783-T-A

29282774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035783-T-C

29282794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035767-T-G

29282797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035764-C-G

29282806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035755-A-G

29282819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035737-G-A

29282835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035722-T-C

29282868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035704-T-C

29283058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035541-G-A

29283058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035541-G-C

29283060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5035539-C-T

29287005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 5033487-C-T

29287777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5033138-A-G

29288293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5032687-G-A

29288496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5032527-G-A

29288496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5032527-G-T

29288521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5032516-G-C

29288677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5032360-G-A

29288719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5032318-G-A

29288734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5032303-G-A

http://identifiers.org/hco/22/GRCh38#29288900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5032137-C-A

29288988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 5032064-A-G

29288989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 5032063-T-A

29289187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5031869-A-G

29289256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5031818-G-A

29289264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5031808-T-A

29289295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5031777-G-A

http://identifiers.org/hco/22/GRCh38#29289300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5031773-C-A

29289343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5031732-G-T

29289469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5031607-A-G

29289469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5031607-A-T

http://identifiers.org/hco/22/GRCh38#29289495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5031581-C-A

29289495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5031581-C-T

http://identifiers.org/hco/22/GRCh38#29289504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5031572-C-A

http://identifiers.org/hco/22/GRCh38#29289505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5031571-C-A

29289505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5031571-C-T

29289507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5031569-T-A

29289616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5031468-A-G

29289660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5031427-T-C

29289722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5031374-C-T

http://identifiers.org/hco/22/GRCh38#29289792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5031310-C-A

http://identifiers.org/hco/22/GRCh38#29289995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5031100-C-A

29289995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5031100-C-T

29290183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5030911-T-C

29290183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5030911-T-G

29290224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5030870-G-A

29290224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5030870-G-T

http://identifiers.org/hco/22/GRCh38#29290287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5030812-C-A

29290287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5030812-C-T

http://identifiers.org/hco/22/GRCh38#29290803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5030295-C-A

http://identifiers.org/hco/22/GRCh38#29290861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5030224-C-A

29290861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5030224-C-G

29290861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5030224-C-T

29290952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5030143-T-C

29291056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5030039-G-A

29291056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5030039-G-T

29291194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5029902-T-G

29291826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5029256-A-T

29291856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5029227-G-A

29292257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5028841-A-G

29292450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5028629-A-T

http://identifiers.org/hco/22/GRCh38#29292629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5028450-C-A

29292629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5028450-C-T

http://identifiers.org/hco/22/GRCh38#29292630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5028449-A-C

29292630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5028449-A-G

http://identifiers.org/hco/22/GRCh38#29292640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5028439-A-C

29292640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5028439-A-G

http://identifiers.org/hco/22/GRCh38#29296245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5022933-A-C

29296245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5022933-A-G

29296463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5022616-T-G

http://identifiers.org/hco/22/GRCh38#29296496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5022583-C-A

http://identifiers.org/hco/22/GRCh38#29296499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5022580-C-A

29296499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5022580-C-G

29296499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5022580-C-T

http://identifiers.org/hco/22/GRCh38#29296519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5022560-C-A

29296519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5022560-C-G

29296519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5022560-C-T

29297745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5021742-G-C

29297745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5021742-G-T

29297750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5021737-T-G

29297795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5021689-G-A

29297806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5021661-T-C

29297925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5021542-G-A

29297925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5021542-G-C

29297970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5021490-T-C

29298687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5021193-G-A

29298714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5021166-C-G

http://identifiers.org/hco/22/GRCh38#29299206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5020749-A-C

29299478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5020585-G-A

29299478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5020585-G-T

29299482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5020581-G-C

29299482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5020581-G-T

29299684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5020393-C-G

29299697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5020380-G-A

29299698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5020379-G-A

29299719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5020358-G-A

29299719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5020358-G-C

29299719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5020358-G-T

29299785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5020292-C-T

29299994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5020157-C-G

29300140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5020083-G-A

29300140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5020083-G-T

29300149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5020074-T-C

29300248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5019982-A-G

http://identifiers.org/hco/22/GRCh38#29300280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#5019950-C-A

29300280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5019950-C-T

29300287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5019943-T-A

29300287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5019943-T-C

29300291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5019939-T-A

29300291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5019939-T-C

29300318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5019913-T-A

29300340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3508
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5019891-T-C