129225103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29768563-G-A

129225103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29768563-G-T

129225247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29768713-G-A

129225247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29768713-G-C

http://identifiers.org/hco/7/GRCh38#129225430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29768896-A-C

129225430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29768896-A-G

129225430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29768896-A-T

http://identifiers.org/hco/7/GRCh38#129225477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#29768946-A-C

129225477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29768946-A-G

129225483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29768956-G-A

129225483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29768956-G-T

http://identifiers.org/hco/7/GRCh38#129225518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29768991-C-A

129225518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29768991-C-G

129225518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29768991-C-T

129225544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769013-A-G

http://identifiers.org/hco/7/GRCh38#129225565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#29769033-C-A

129225565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769033-C-G

129225565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769033-C-T

129225807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769255-C-T

129226143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769559-G-C

129226166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769582-G-A

129226214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769629-G-C

129226232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29769634-C-T

129226278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29769660-T-C

129226929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29770230-A-G

129227131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29770422-A-T

129227136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29770427-A-G

http://identifiers.org/hco/7/GRCh38#129227643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29770644-C-A

129228956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29772379-T-C

129229916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29773159-C-T

129230077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29773267-T-A

129230554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29773737-C-T

129230779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29773913-T-G

129231452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29774447-A-G

129231698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29774644-T-A

129231763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29774721-C-T

129232060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29775151-C-T

129232132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29775465-A-G

129232700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29776045-C-T

http://identifiers.org/hco/7/GRCh38#129232737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29776090-C-A

129232849-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29776204-T-G

129236705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29780769-C-T

129236706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29780770-G-A

http://identifiers.org/hco/7/GRCh38#129236843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29780919-C-A

129236843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29780919-C-T

129236912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29780992-G-A

129240357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29783790-C-T

129240547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29783990-A-G

129240795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29784215-T-C

http://identifiers.org/hco/7/GRCh38#129240829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29784249-C-A

129240829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29784249-C-T

129240903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29784319-C-T

129241087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29784758-C-G

129241087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29784758-C-T

129241136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29784810-T-G

129241170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29784843-T-G

129241239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29784914-G-T

129258917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29789030-G-A

129259351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29790061-T-G

129261360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29792232-G-T

129261439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29792316-G-A

129270270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29795134-G-A

129283513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29802330-G-T

129283995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29802911-T-C

129284085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29802990-G-C

129284150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29803057-G-A

129284794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29803500-A-T

129285094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29803757-A-G

129285094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29803757-A-T

129285475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29804131-C-T

129285488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29804144-G-A

129287288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29805421-C-G

129287441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29805567-C-T

129290917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29809864-G-C

129293207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29811641-G-A

129293299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29811722-G-A

129293348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29811771-A-G

129293432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29811851-G-A

129293482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29811999-C-G

129293512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29812041-C-T

129293783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29812362-T-C

129294193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29812777-G-A

129294391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29812962-G-T

129294483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29813054-A-G

129294668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29814310-T-C

129295136-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29814713-G-C

129295363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29814940-T-G

129296580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29817787-A-G

129296918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29817966-T-G

129296931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29817995-T-A

129296962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29818026-C-T

129297052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29818116-C-T

129297122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29818201-G-T

129297790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29818695-G-A

129297852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29818757-A-G

129298466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29819511-T-G

129298499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29819544-T-C

129315277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29820971-T-C

http://identifiers.org/hco/7/GRCh38#129315404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29821066-C-A

129316019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29821818-A-G

129316570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29822496-T-C

129332529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 29827429-C-G

129342037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29831407-A-G

129342566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29832533-G-A

129349297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29836170-T-C

129351079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29838218-A-G

129351222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29838343-G-A

129351277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29838388-G-T

129351722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29838744-G-A

129351722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29838744-G-T

129351875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29838887-C-T

129351934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29838979-G-C

129352137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29839383-T-C

129352419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29839732-C-T

129352420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29839733-A-G

129352616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29840075-C-T

http://identifiers.org/hco/7/GRCh38#129352934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29840396-A-C

129352934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29840396-A-T

http://identifiers.org/hco/7/GRCh38#129353664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29841478-C-A

129354569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29842620-G-T

129354815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29842883-C-T

129356150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29845993-C-T

129356329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29846152-C-G

129356650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29846502-A-G

http://identifiers.org/hco/7/GRCh38#129356652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29846504-C-A

129356652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29846504-C-G

129362175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29849493-A-G

http://identifiers.org/hco/7/GRCh38#129362572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29849968-C-A

http://identifiers.org/hco/7/GRCh38#129362633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29850002-A-C

129362633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29850002-A-T

129363215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29850494-A-G

129363383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29850656-T-C

http://identifiers.org/hco/7/GRCh38#129364820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29851084-C-A

129365014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29851261-A-G

http://identifiers.org/hco/7/GRCh38#129365055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29851306-A-C

129365055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29851306-A-G

129365278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29851534-A-G

129365420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29851639-C-T

129367818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29853441-T-A

129368167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29853793-A-G

129368250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29853841-A-G

http://identifiers.org/hco/7/GRCh38#129368288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#29853877-C-A

129368288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29853877-C-T

129368305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29853895-G-A

129368305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 29853895-G-T

129368345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29853935-T-A

129369413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29855201-G-C

129369585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29855341-C-G

129370165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29855925-A-G

129370167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29855927-A-G

129370191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29855951-G-A

129370818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29856168-C-T

129371040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29856360-G-A

http://identifiers.org/hco/7/GRCh38#129371185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29856502-A-C

129371305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29856618-C-T

129371634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29856927-C-T

129371859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29857167-G-A

129372114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29857272-A-G

129375515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29859354-A-G

129375515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29859354-A-T

http://identifiers.org/hco/7/GRCh38#129375657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29859483-C-A

129375657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29859483-C-T

129375694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29859522-G-A

129375694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29859522-G-T

129376598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29860383-T-C

129376864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29860688-T-C

129376933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29860747-C-T

129377301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29861094-C-T

129377633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29861421-C-T

http://identifiers.org/hco/7/GRCh38#129377750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29861534-C-A

129377963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29861696-G-T

129378001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29861709-A-G

129378332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29861762-T-C

129378879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29862127-T-C

129378898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29862146-T-C

129379297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29862765-G-A

http://identifiers.org/hco/7/GRCh38#129379530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29863068-C-A

129379530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29863068-C-G

129379530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29863068-C-T

http://identifiers.org/hco/7/GRCh38#129379570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29863091-C-A

129379570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29863091-C-T

129379766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29863267-T-G

129379948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29863441-C-T

129379965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29863458-T-C

129380282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29863925-A-G

129380398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29864030-G-T

129381141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29864617-A-G

129381239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29864714-C-G

129381268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29864742-A-G

129381286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29864754-C-T

http://identifiers.org/hco/7/GRCh38#129386787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29868230-C-A

129388080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 29868878-G-T

129388110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29868908-T-C

129388137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29868930-T-C

129388322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29869106-G-A

129388322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29869106-G-T

129388499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29869990-A-G

129388514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29870005-T-G

129388598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29870089-G-C

129388681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29870172-A-G

129388707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29870221-T-G

129388711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29870225-T-C

129388829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29870330-G-T

129388861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29870362-T-C

129388900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29870399-C-T

129389099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29870610-G-A

129389230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29870732-A-T

129389516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29871077-A-T

http://identifiers.org/hco/7/GRCh38#129389521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29871082-A-C

http://identifiers.org/hco/7/GRCh38#129389528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29871089-C-A

129389528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29871089-C-T

129389597-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29871148-C-G

129389597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29871148-C-T

http://identifiers.org/hco/7/GRCh38#129389611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29871162-C-A

129389680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29871231-G-A

129389707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29871258-T-C

129389707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29871258-T-G

129389741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 29871292-T-C

129389785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29871321-G-A

129389785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29871321-G-T

129389799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29871335-T-A

129389800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29871336-T-C

129389837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29871362-T-C

129391956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29874376-G-T

129392125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29874498-C-T

129397112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29878313-G-T

http://identifiers.org/hco/7/GRCh38#129397133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29878334-A-C

129397173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29878482-T-A

129397173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29878482-T-C

129397173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29878482-T-G

129397251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29878557-G-A

129397251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29878557-G-T

129397392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29878696-A-G

129397506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29878802-C-T

129398801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29879429-A-G

129398968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29879577-C-G

129398982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29879584-G-A

129398982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29879584-G-C

http://identifiers.org/hco/7/GRCh38#129400169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29880461-C-A

129400169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29880461-C-T

129400176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29880468-G-A

129400176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29880468-G-T

129400202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29880484-T-C

http://identifiers.org/hco/7/GRCh38#129400497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29880741-C-A

129400506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29880750-A-G

http://identifiers.org/hco/7/GRCh38#129400519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29880763-C-A

129400885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29881145-A-G

129401113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29881297-C-T

129401200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29881341-T-C

129401235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29881370-T-A

129401235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29881370-T-C

129401636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29881692-G-A

http://identifiers.org/hco/7/GRCh38#129401662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29881722-A-C

129401838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29881891-G-A

129402034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29882076-G-A

129402242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29882599-G-A

129402481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29882830-G-T

129402526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29882874-C-T

129402895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29883205-C-T

129403240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29883506-T-A

http://identifiers.org/hco/7/GRCh38#129404000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29883868-C-A

129404000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29883868-C-T

129404981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29886000-G-A

129404981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29886000-G-T

129405005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29886023-A-G

129405053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29886071-G-T

129405100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29886120-G-A

129405323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29890332-T-C

129405323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29890332-T-G

129405408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29890403-T-C

129405461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29890450-T-G

http://identifiers.org/hco/7/GRCh38#129405476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29890465-C-A

129405476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29890465-C-T

129405504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 29890492-A-G

129405553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29890547-G-A

129405553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29890547-G-T

129405581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29890566-T-G

http://identifiers.org/hco/7/GRCh38#129405772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29890604-C-A

129405773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29890605-A-G

129405975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29890819-G-A

129405993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29890831-T-G

http://identifiers.org/hco/7/GRCh38#129406252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29891073-C-A

129406252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29891073-C-G

http://identifiers.org/hco/7/GRCh38#129406261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29891082-A-C

129406261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29891082-A-G

129406261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29891082-A-T

129406479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29891301-G-A

129406499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29891321-C-T

129406501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29891331-C-T

129406625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29891445-G-A

129406671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29891474-G-A

129407851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29893008-C-T

129407852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29893009-T-C

129408034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29893236-A-G

129408524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29893923-A-G

129408892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29894317-T-G

129409054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29894348-T-G

129409269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29894501-T-C

http://identifiers.org/hco/7/GRCh38#129409392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29894747-A-C

129409392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29894747-A-G

129409435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29894779-G-A

http://identifiers.org/hco/7/GRCh38#129409559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29894901-C-A

129409561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29894903-T-A

http://identifiers.org/hco/7/GRCh38#129409605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29894947-C-A

129409605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29894947-C-T

129409645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29894989-G-A

129409645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29894989-G-C

129409645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29894989-G-T

129413723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29896465-T-C

129414168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29896809-G-A

129414202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29896840-C-T

129414381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29896992-A-G

129414809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29897108-C-T

129414827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29897126-G-A

129414912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29897209-G-A

129416018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29897927-G-A

129416360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29898175-G-A

129417236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29898357-A-G

129417347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29898457-G-C

129417583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29898685-C-G

129417698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29898779-G-T

129419537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29900549-G-C

129419848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29900749-G-C

129420170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29901156-T-C

129420170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29901156-T-G

129420353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29901350-A-G

129420353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29901350-A-T

129421872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29902250-A-G

129421872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29902250-A-T

129422893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29903241-C-T

129422999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29903354-C-T

http://identifiers.org/hco/7/GRCh38#129423043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29903399-C-A

129423068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29903424-G-A

129423068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29903424-G-T

129423324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29903663-G-A

129423480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29903888-G-A

129424006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 29904564-A-G

129424066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29904616-A-G

129424437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29904737-G-C

129424632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29904916-T-C

129425025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29906642-T-C

http://identifiers.org/hco/7/GRCh38#129425185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29906799-A-C

129425185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29906799-A-G

http://identifiers.org/hco/7/GRCh38#129426326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29908241-C-A

129426395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29908308-G-A

129426415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 29908324-A-T

129426501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 29908404-A-T

129427075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29909078-G-A

129427075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29909078-G-T

129427160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29909161-T-C

129427227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29909228-G-A

129427227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29909228-G-C

129427227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29909228-G-T

129427280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29909282-G-A

129427280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29909282-G-T

129427882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29909867-T-C

129427910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29909893-G-T

http://identifiers.org/hco/7/GRCh38#129427957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29909927-C-A

129427957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29909927-C-T

129428003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29909970-G-T

129428019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29909986-A-T

http://identifiers.org/hco/7/GRCh38#129428063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29910015-C-A

129428128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29910062-G-A

129428132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29910066-T-C

129428221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29910246-C-T

129428230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29910255-G-A

129428230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29910255-G-T

http://identifiers.org/hco/7/GRCh38#129428264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29910309-C-A

129428295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29910340-T-G

http://identifiers.org/hco/7/GRCh38#129428577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29910604-C-A

129428605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29910628-A-G

129428616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29910638-C-T

http://identifiers.org/hco/7/GRCh38#129428662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29910681-C-A

129428662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29910681-C-T

129428822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29910841-G-T

129428925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29910925-G-C

129428961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29911151-G-T

129429083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29911255-T-C

129429136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29911288-T-A

http://identifiers.org/hco/7/GRCh38#129429139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29911291-A-C

129429139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29911291-A-G

129429150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29911302-C-T

http://identifiers.org/hco/7/GRCh38#129429197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29911348-C-A

129429295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29911529-A-G

http://identifiers.org/hco/7/GRCh38#129429398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29911649-C-A

129429428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29911679-G-C

129429432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29911683-A-G

http://identifiers.org/hco/7/GRCh38#129430027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#29912124-A-C

129430027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22204
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 29912124-A-G