158536544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307052-G-A

158536544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307052-G-T

158536552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307060-G-A

158536552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307060-G-T

158536641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307139-G-A

158536641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307139-G-T

http://identifiers.org/hco/6/GRCh38#158536653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6307152-C-A

158536653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307152-C-T

http://identifiers.org/hco/6/GRCh38#158536654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6307153-C-A

158536654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307153-C-T

158536676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307175-G-A

158536676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307175-G-T

158536678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307177-G-A

158536678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307177-G-T

158536685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307184-G-A

158536685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307184-G-T

158536720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307215-G-A

158536720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307215-G-C

158536720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5 prime UTR variant
orthologous variants: 6307215-G-T

http://identifiers.org/hco/6/GRCh38#158536766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6307250-C-A

158536766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 6307250-C-T

http://identifiers.org/hco/6/GRCh38#158536795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6307279-C-A

158536795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 6307279-C-T

158536827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 6307311-G-T

http://identifiers.org/hco/6/GRCh38#158536846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6307330-A-C

158536846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 6307330-A-G

http://identifiers.org/hco/6/GRCh38#158536906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#6307359-C-A

158536913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, undefined
orthologous variants: 6307366-G-A

158536934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6307386-G-A

158536939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6307391-C-T

158536944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6307396-G-A

158536985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6307404-G-A

158537108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6307479-C-T

http://identifiers.org/hco/6/GRCh38#158537127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#6307498-C-A

158537127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, undefined
orthologous variants: 6307498-C-T

158537209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6307571-G-A

158537232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, undefined
orthologous variants: 6307603-C-T

158537265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6307636-G-C

158537452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, undefined
orthologous variants: 6307834-T-C

158537874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6308254-A-G

158539289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6309861-G-A

158539410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6309968-C-T

http://identifiers.org/hco/6/GRCh38#158539984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6310492-C-A

158539991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6310499-G-A

158540131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6310613-G-A

158540138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6310620-T-C

158540268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6310748-G-A

158545203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, undefined
orthologous variants: 6317473-A-G

158545209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, undefined
orthologous variants: 6317479-A-G

158547467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6318716-G-A

158547467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6318716-G-C

http://identifiers.org/hco/6/GRCh38#158547560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6318785-C-A

158547607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6318821-C-G

158548222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, undefined
orthologous variants: 6319643-G-A

158548794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6320191-A-G

158548884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6320273-C-T

158548996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6320378-C-G

158548996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron variant
orthologous variants: 6320378-C-T

http://identifiers.org/hco/6/GRCh38#158560117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6320774-A-C

158560117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6320774-A-G

http://identifiers.org/hco/6/GRCh38#158560120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6320777-C-A

158560120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6320777-C-G

158560120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6320777-C-T

158560124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6320781-G-A

158560195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6320828-G-A

http://identifiers.org/hco/6/GRCh38#158560199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6320832-C-A

158560199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6320832-C-T

158560266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6320884-C-T

158560596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6321033-C-T

158560638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6321059-G-T

158560788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6321180-T-C

158560847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6321230-A-G

158560894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6321271-C-T

158560929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6321305-G-A

158560929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6321305-G-T

158560956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6321314-A-G

158560964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6321322-G-A

158561251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6321481-T-C

158561259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 6321489-C-G

158561544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6321708-G-C

158563726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6322680-A-G

158564184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6322834-C-T

158564412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6323014-C-G

158564445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6323056-C-G

158565359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6324385-A-G

158565532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6324577-A-T

158565648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6324656-T-G

158565714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6324703-G-C

158565990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6324981-T-C

158566034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6325006-T-C

158566067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6325040-A-G

158567202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6325863-A-G

158567245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6325910-C-T

158573144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330628-G-T

158573174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330660-C-T

158573199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330680-C-T

158573213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330687-C-T

158573286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330758-G-A

158573286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330758-G-T

http://identifiers.org/hco/6/GRCh38#158573288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6330760-C-A

158573288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330760-C-T

158573295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330767-A-G

158573295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330767-A-T

158573308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330779-T-A

158573308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330779-T-C

http://identifiers.org/hco/6/GRCh38#158573324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6330795-C-A

158573324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330795-C-T

158573392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330845-G-A

158573432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: 6330885-G-C

158573432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: 6330885-G-T

http://identifiers.org/hco/6/GRCh38#158573441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/17/GRCm39#6330894-C-A

158573441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6330894-C-T

158573443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6330896-C-G

158573443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6330896-C-T

158573444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6330897-G-A

158573444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6330897-G-T

http://identifiers.org/hco/6/GRCh38#158573454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6330907-C-A

158573454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6330907-C-T

158573462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6330915-T-C

158573462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6330915-T-G

158573471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6330924-G-T

158573495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6330948-T-G

158573505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6330958-A-G

158573516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6330969-G-A

158573516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6330969-G-T

http://identifiers.org/hco/6/GRCh38#158573543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6330995-C-A

158573543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330995-C-G

158573543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6330995-C-T

http://identifiers.org/hco/6/GRCh38#158573591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6331022-C-A

158573591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6331022-C-G

http://identifiers.org/hco/6/GRCh38#158573592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6331023-A-C

http://identifiers.org/hco/6/GRCh38#158573605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6331035-C-A

158573605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6331035-C-T

158573625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6331037-G-A

158573625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6331037-G-T

158573640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6331052-G-A

158573651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6331076-C-T

158573662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6331088-T-A

158573678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6331103-C-T

158573679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6331104-G-A

158574066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6332093-C-T

158574170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6332191-T-C

158574191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6332210-T-A

http://identifiers.org/hco/6/GRCh38#158574198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6332217-A-C

158574198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6332217-A-G

158574250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6332270-T-G

158574301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6332303-C-G

158574301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6332303-C-T

http://identifiers.org/hco/6/GRCh38#158574347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6332346-A-C

158574347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6332346-A-G

158574414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6332421-A-G

158574468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6332477-T-C

158574558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6332557-A-G

158575168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6333301-G-A

158575172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6333305-C-T

http://identifiers.org/hco/6/GRCh38#158575344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6333469-A-C

158575349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6333474-A-G

158580737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6337016-G-T

http://identifiers.org/hco/6/GRCh38#158580797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6337063-C-A

158580914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6337175-T-C

158581023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6337282-G-T

158581037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6337296-T-C

http://identifiers.org/hco/6/GRCh38#158581128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6337367-C-A

158581128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6337367-C-T

158581652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6337899-G-T

http://identifiers.org/hco/6/GRCh38#158581745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6338029-C-A

158581745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6338029-C-G

158581745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6338029-C-T

158581786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6338053-T-C

158581821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6338085-A-G

158581948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6338260-C-G

158581956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6338268-T-C

158582331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6338603-C-G

158583839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339146-A-G

http://identifiers.org/hco/6/GRCh38#158583875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6339166-C-A

158583875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339166-C-T

158583892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339187-A-G

158583909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339203-C-T

158583920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339214-G-T

158583935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339228-T-C

158583998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6339302-T-C

158584015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6339319-C-T

158584019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6339323-T-C

158584020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6339324-G-C

158584068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339359-T-C

158584098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339388-T-G

http://identifiers.org/hco/6/GRCh38#158584111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6339408-C-A

158584111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339408-C-T

http://identifiers.org/hco/6/GRCh38#158584118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6339415-A-C

158584118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339415-A-G

158584179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339458-A-G

158584179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339458-A-T

158584591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339742-G-T

158584593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339744-A-G

158584602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339753-G-A

158584676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339804-G-A

http://identifiers.org/hco/6/GRCh38#158584708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6339828-A-C

158584788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339869-A-G

158584808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339889-A-G

158584812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6339893-T-C

158585016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6340603-T-C

158585054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6340627-G-T

http://identifiers.org/hco/6/GRCh38#158585235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6340760-C-A

158585235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6340760-C-G

158585235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6340760-C-T

158585236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6340761-A-G

158585245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6340770-C-T

158585248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6340773-T-C

158585257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6340782-T-A

158585257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6340782-T-C

158585267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6340792-G-A

158585267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6340792-G-C

158585353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6340881-A-G

158585374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6340902-G-A

http://identifiers.org/hco/6/GRCh38#158585415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6340943-C-A

158585415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6340943-C-T

158585878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6341634-G-T

158585949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6341707-C-T

158586120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6341879-A-G

158586132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6341893-A-G

158586393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6342307-T-A

158586523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6342436-A-G

158586537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6342450-G-A

158586647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6342586-T-C

158587356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6343205-A-G

158587370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6343218-T-C

158587420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6343266-C-T

158587438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6343284-C-T

158587467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6343313-A-T

158587498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6343348-A-T

158587895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6344251-G-A

158587895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6344251-G-T

158588067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6344414-G-A

158589182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6344762-G-C

158589182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6344762-G-T

158589343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6344907-C-T

http://identifiers.org/hco/6/GRCh38#158589522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6345058-C-A

158589552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6345094-G-A

158589552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6345094-G-T

158589576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6345108-T-C

158589576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6345108-T-G

158589598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6345130-G-T

158589922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6345396-G-T

158605295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6346025-G-A

158605295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6346025-G-T

158605313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6346043-G-A

158605361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6346091-G-A

158605361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6346091-G-T

158605376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6346108-G-A

158605376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6346108-G-T

158605384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6346113-C-G

158605970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6346558-C-T

158606490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347052-C-T

158606587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347150-C-T

158606624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347180-A-G

http://identifiers.org/hco/6/GRCh38#158606652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6347208-A-C

158606966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347343-G-T

158606973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347350-C-T

158607116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347418-G-A

158607116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347418-G-T

158607148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347445-T-A

158607148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347445-T-G

158607153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347450-A-G

158607153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347450-A-T

158607159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347458-A-G

158607231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347490-A-G

158607750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347717-G-A

158607812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347770-G-A

158607873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347804-C-T

158607953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347872-C-T

158607957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6347876-C-T

158608133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6348042-C-T

158608392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6348186-C-T

158608493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6348285-G-T

http://identifiers.org/hco/6/GRCh38#158608643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6348405-A-C

158608643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6348405-A-G

158608703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6348468-T-C

158608733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6348498-G-A

158608733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6348498-G-C

158608733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6348498-G-T

158608770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6348540-G-A

158608770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6348540-G-C

158623339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6349436-G-A

158623418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6349510-A-G

158623438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6349530-G-A

158623438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6349530-G-T

158623475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6349565-G-A

158623475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6349565-G-C

158623475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6349565-G-T

158623568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6349656-T-C

http://identifiers.org/hco/6/GRCh38#158623645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6349733-A-C

158623645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6349733-A-G

158624221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350458-C-T

158624222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350459-G-A

158624273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350511-C-T

158624465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350714-G-A

158624530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350754-C-T

158624604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350782-C-T

158624687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350857-C-T

158624690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350860-C-T

158624908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6350990-T-A

158624969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6351037-G-A

http://identifiers.org/hco/6/GRCh38#158625016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6351088-C-A

158625016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6351088-C-T

http://identifiers.org/hco/6/GRCh38#158625028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6351100-C-A

158625041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6351112-T-G

158625045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6351116-G-A

158625134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6351197-G-A

158625202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6351265-T-C

158625229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6351279-G-A

158625348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6351322-A-G

158625409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6351368-G-A

158625447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6351421-G-A

158625623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6351602-A-G

158625662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6351653-A-G

158625665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6351656-T-C

http://identifiers.org/hco/6/GRCh38#158628405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6353493-C-A

158628405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6353493-C-T

158629022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354093-G-A

158629145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354191-T-C

158629470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354342-G-A

158629470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354342-G-C

158629559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6354385-T-C

158629559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6354385-T-G

158629581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354407-A-G

158629581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354407-A-T

http://identifiers.org/hco/6/GRCh38#158629589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6354415-C-A

158629589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354415-C-T

158629607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354431-C-T

158629625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354439-T-C

158629692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354484-G-A

158629860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354640-G-A

158629860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354640-G-T

158629933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354682-A-T

158629943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354692-G-C

158629943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354692-G-T

http://identifiers.org/hco/6/GRCh38#158629944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6354693-C-A

158629944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354693-C-T

158631293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354822-T-C

158631293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6354822-T-G

158631397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 6354926-C-T

158631399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6354928-T-C

158631399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6354928-T-G

158631435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6354946-G-A

158631440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6354951-G-A

158631571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6355054-T-C

158631573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6355056-T-C

158631850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6355684-A-G

158631850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6355684-A-T

158631880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6355714-A-G

158631960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355794-T-G

158632025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355860-G-A

158632025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6355860-G-T

158632152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6355992-G-A

158632152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6355992-G-T

158632182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356024-T-C

http://identifiers.org/hco/6/GRCh38#158632231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6356070-C-A

158632250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356090-T-A

158632266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6356106-G-A

158632266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6356106-G-T

158632282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356123-C-G

158632349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356182-T-A

http://identifiers.org/hco/6/GRCh38#158632368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6356207-C-A

158632368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356207-C-T

158632373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356222-T-C

158632387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356237-C-G

158632435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356287-T-C

http://identifiers.org/hco/6/GRCh38#158632461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#6356298-C-A

158632461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6356298-C-T

http://identifiers.org/hco/6/GRCh38#158632503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#6356349-C-A

158632523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356372-T-C

158632543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356390-G-A

158632543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356390-G-T

http://identifiers.org/hco/6/GRCh38#158632588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6356429-C-A

158632606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356446-T-C

158632720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356543-G-T

158632727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356550-T-C

158632727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356550-T-G

158632745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356569-A-G

158632767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356594-A-G

158632782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356609-G-T

158633365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356850-T-C

158633367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356852-C-T

158633370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356855-A-G

http://identifiers.org/hco/6/GRCh38#158633434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6356871-C-A

158633434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356871-C-T

158633510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356931-A-G

158633560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356981-T-C

158633561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356982-G-A

158633700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357077-A-G

158633719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357096-T-A

158633720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357097-A-T

158633733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357117-A-G

http://identifiers.org/hco/6/GRCh38#158633756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6357142-C-A

158633756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357142-C-T

http://identifiers.org/hco/6/GRCh38#158633825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6357210-A-C

http://identifiers.org/hco/6/GRCh38#158633841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6357226-C-A

158634148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357492-G-T

http://identifiers.org/hco/6/GRCh38#158634268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6357556-A-C

http://identifiers.org/hco/6/GRCh38#158634282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6357570-C-A

158634298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357586-G-A

158634323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357609-G-A

158634323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357609-G-C

http://identifiers.org/hco/6/GRCh38#158634391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6357660-A-C

158634410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357673-G-A

158634410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357673-G-T

158634523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357798-A-G

158634532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357802-G-T

158634569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357838-T-G

158634587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357856-T-C

158634680-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357937-T-A

158634680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357937-T-C

158634684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357941-T-A

158634684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357941-T-C

158634698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357955-G-C

158634698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357955-G-T

158634701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6357958-T-G

http://identifiers.org/hco/6/GRCh38#158634735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6357990-C-A

158634758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6358008-A-G

158634784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6358033-C-T

http://identifiers.org/hco/6/GRCh38#158634884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#6358114-A-C

158634884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6358114-A-G

158634884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6358114-A-T

158634963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6358186-T-C

158634963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6358186-T-G

158635000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6358201-C-T

158635018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6358219-G-A

158635018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6358219-G-C

158635018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6358219-G-T

158635123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20958
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6358328-T-C